2-32148690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148690
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148690
    reference: chr 2
allele count: 1
allele frequency: 6.663113006396588e-5
allele num: 15008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2711G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.*23G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2711G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19681G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-32148695-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148695
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148695
    reference: chr 2
allele count: 8
allele frequency: 5.248655032148012e-4
allele num: 15242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2716A>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.*18A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2716A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19676A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2716A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2716A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2716A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2716A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2716A>C
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

2-32148699-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148699
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148699
    reference: chr 2
allele count: 1
allele frequency: 6.513809275664408e-5
allele num: 15352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.*14T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19672T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2720T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2720T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2720T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2720T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2720T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2720T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2720T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-32148721-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148721
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148721
    reference: chr 2
allele count: 1
allele frequency: 6.233636703652911e-5
allele num: 16042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2742A>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2742A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2742A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.295A>T
  hgvsp: ENSP00000385321.3:p.Ile99Phe
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2742A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19650A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2742A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2742A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2742A>T
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile99Phe
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

2-32148737-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148737
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148737
    reference: chr 2
allele count: 1
allele frequency: 6.146281499692685e-5
allele num: 16270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2758A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2758A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.279A>G
  hgvsp: ENST00000407893.3:c.279A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2758A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2758A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2758A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19634A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2758A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2758A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg93Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

2-32148755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148755
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148755
    reference: chr 2
allele count: 3
allele frequency: 1.835760616815567e-4
allele num: 16342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19616C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.261C>T
  hgvsp: ENST00000407893.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2776C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2776C>T
  variant of: http://identifiers.org/hgnc/24590
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe87Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

2-32148766-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148766
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148766
    reference: chr 2
allele count: 1
allele frequency: 6.117704637220115e-5
allele num: 16346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2787C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.250C>G
  hgvsp: ENSP00000385321.3:p.Leu84Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2787C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19605C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2787C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2787C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2787C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2787C>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2787C>G
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu84Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-32148814-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32148814
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32148814
    reference: chr 2
allele count: 24
allele frequency: 1.532958610117527e-3
allele num: 15656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-2835G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.213-2835G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.286-2835G>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.222-2835G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.247-2835G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.213-11G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+19557G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.213-2835G>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.383-2835G>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

2-32157087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157087
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157087
    reference: chr 2
allele count: 11
allele frequency: 9.097074050182768e-5
allele num: 120918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+49G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11108G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+49G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+49G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+49G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+49G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11284G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+49G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+49G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23785
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30593
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-32157092-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157092
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157092
    reference: chr 2
allele count: 8
allele frequency: 6.613428566704694e-5
allele num: 120966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11113T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+44T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11279T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+44T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+44T>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+44T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+44T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+44T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+44T>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23914
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-32157097-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157097
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157097
    reference: chr 2
allele count: 2
allele frequency: 1.653302471687195e-5
allele num: 120970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+39A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+39A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11274A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+39A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11118A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+39A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+39A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+39A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+39A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

2-32157108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157108
    reference: chr 2
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+28G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11129G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11263G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24245
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6653
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32698
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-32157109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157109
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157109
    reference: chr 2
allele count: 3
allele frequency: 2.478396642598681e-5
allele num: 121046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11262C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+27C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+27C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+27C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11130C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+27C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+27C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+27C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+27C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14489
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8974
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

2-32157112-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157112
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157112
    reference: chr 2
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+24A>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+24A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11133A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11259A>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6651
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32935
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-32157117-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157117
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157117
    reference: chr 2
allele count: 21
allele frequency: 1.733560071984018e-4
allele num: 121138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11254T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+19T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+19T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+19T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+19T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+19T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11138T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+19T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+19T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

2-32157120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157120
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157120
    reference: chr 2
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+16T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+16T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11141T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+16T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+16T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+16T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+16T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11251T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+16T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33089
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6643
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-32157123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157123
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157123
    reference: chr 2
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11144G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+13G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+13G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11248G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-32157126-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157127
    reference: chr 2
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11148dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+9dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11244dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+9dupT
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6643
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2542
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

2-32157126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157126
    reference: chr 2
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11147G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.221+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.246+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.212+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.212+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.285+10G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.382+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.212+10G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11245G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3692
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

2-32157140-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157140
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157140
    reference: chr 2
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11231A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.217A>G
  hgvsp: ENSP00000368691.3:p.Ile73Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11161A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.242A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.378A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.208A>G
  hgvsp: ENSP00000385557.1:p.Ile70Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.208A>G
  hgvsp: ENSP00000385321.3:p.Ile70Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.281A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.208A>G
  hgvsp: ENSP00000295065.4:p.Ile70Val
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile70Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

2-32157142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157142
    reference: chr 2
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.240C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.206C>T
  hgvsp: ENSP00000385557.1:p.Ser69Phe
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11163C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.206C>T
  hgvsp: ENSP00000295065.4:p.Ser69Phe
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.279C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.206C>T
  hgvsp: ENSP00000385321.3:p.Ser69Phe
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.215C>T
  hgvsp: ENSP00000368691.3:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.376C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11229C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser69Phe
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

2-32157144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157144
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157144
    reference: chr 2
allele count: 57
allele frequency: 4.700953386335896e-4
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.144-11165G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.213G>A
  hgvsp: ENST00000379383.3:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.204G>A
  hgvsp: ENST00000407893.3:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.374G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.204G>A
  hgvsp: ENST00000295065.5:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.277G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11227G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.238G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.204G>A
  hgvsp: ENST00000404530.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14497
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro68Pro
num of homozygotes: 1
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/2-32157180-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157180
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157180
    reference: chr 2
allele count: 5
allele frequency: 4.125004125004125e-5
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.338G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.177G>T
  hgvsp: ENST00000379383.3:c.177G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11191G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.168G>T
  hgvsp: ENST00000295065.5:c.168G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.202G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.241G>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.168G>T
  hgvsp: ENST00000404530.1:c.168G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.168G>T
  hgvsp: ENST00000407893.3:c.168G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11191G>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly56Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-32157189-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157189
    reference: chr 2
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.329G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.159G>T
  hgvsp: ENST00000295065.5:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.159G>T
  hgvsp: ENST00000404530.1:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.159G>T
  hgvsp: ENST00000407893.3:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11182G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.232G>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.168G>T
  hgvsp: ENST00000379383.3:c.168G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11182G>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.193G>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6610
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2541
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr53Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-32157189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157189
    reference: chr 2
allele count: 2
allele frequency: 1.650437365901964e-5
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.159G>A
  hgvsp: ENST00000404530.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.193G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.159G>A
  hgvsp: ENST00000407893.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11182G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.168G>A
  hgvsp: ENST00000379383.3:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.159G>A
  hgvsp: ENST00000295065.5:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.232G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.329G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11182G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2541
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr53Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

2-32157206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157206
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157206
    reference: chr 2
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11165A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-2A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-2A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11165A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32822
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: c.144-2A>G
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-32157213-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157213
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157212
    reference: chr 2
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11157delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-10delT
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-10delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11157delT
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: CA
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

2-32157217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157217
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157217
    reference: chr 2
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-13T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-13T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11154T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-13T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11154T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-13T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-13T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-13T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-13T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3647
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

2-32157221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157221
    reference: chr 2
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11150A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11150A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-17A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-17A>G
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31436
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

2-32157224-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157224
    reference: chr 2
allele count: 1
allele frequency: 8.307717869901138e-6
allele num: 120370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11147A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-20A>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-20A>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11147A>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8527
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-32157230-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157230
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157231
    reference: chr 2
allele count: 43
allele frequency: 3.577549628101236e-4
allele num: 120194
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-27dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-27dupT
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-27dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11140dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-27dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11140dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-27dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-27dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-27dupT
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 22114
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-32157240-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157240
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157240
    reference: chr 2
allele count: 2
allele frequency: 1.670146137787057e-5
allele num: 119750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-36T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-36T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11131T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11131T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-36T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-36T>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-36T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-36T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-36T>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18099
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

2-32157242-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157242
    reference: chr 2
allele count: 1
allele frequency: 8.359945827551038e-6
allele num: 119618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11129A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-38A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11129A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-38A>G
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6860
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21451
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

2-32157248-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32157248
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32157248
    reference: chr 2
allele count: 1
allele frequency: 8.399267583866688e-6
allele num: 119058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.178-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.144-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.314-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+11123A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.144-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.153-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.217-44A>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.144-44A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+11123A>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15218
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

2-32168320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168320
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168320
    reference: chr 2
allele count: 12
allele frequency: 1.014507456629806e-4
allele num: 118284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+51C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+51C>T
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

2-32168320-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168320
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168320
    reference: chr 2
allele count: 1
allele frequency: 8.454228805248384e-6
allele num: 118284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+51C>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+51C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+51C>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-32168325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168325
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168325
    reference: chr 2
allele count: 1
allele frequency: 8.411277841329655e-6
allele num: 118888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+46G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+46G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+46G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-32168333-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168333
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168334
    reference: chr 2
allele count: 30
allele frequency: 2.52177129215561e-4
allele num: 118964
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+37dupT
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+37dupT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+37dupT
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/2-32168340-CAAAACA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168334
    reference: chr 2
allele count: 4
allele frequency: 3.355535795178095e-5
allele num: 119206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+25_216+30delTGTTTT
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+25_143+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+25_143+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+25_177+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+25_82+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+25_313+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+25_152+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+25_143+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+25_143+30delTGTTTT
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: CAAAACA
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-32168340-CAAAACAAAAACA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168328
    reference: chr 2
allele count: 1
allele frequency: 8.388839487945237e-6
allele num: 119206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37726
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3023
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3037
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: CAAAACAAAAACA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-32168342-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168342
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168342
    reference: chr 2
allele count: 1
allele frequency: 8.380543729677181e-6
allele num: 119324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+29T>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+29T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+29T>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

2-32168353-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168353
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168353
    reference: chr 2
allele count: 1
allele frequency: 8.356732183446986e-6
allele num: 119664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+18T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+18T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+18T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ

2-32168363-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168363
    reference: chr 2
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216+8T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143+8T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143+8T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6832
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
hgvs: c.143+8T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum

2-32168371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168371
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168371
    reference: chr 2
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.152C>T
  hgvsp: ENSP00000368691.3:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.143C>T
  hgvsp: ENSP00000385321.3:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.143C>T
  hgvsp: ENSP00000385557.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.143C>T
  hgvsp: ENSP00000400795.2:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.143C>T
  hgvsp: ENSP00000295065.4:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.82C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.177C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.313C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.216C>T
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro48Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-32168374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168374
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168374
    reference: chr 2
allele count: 2
allele frequency: 1.659640853719255e-5
allele num: 120508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.213C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.140C>T
  hgvsp: ENSP00000295065.4:p.Ala47Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.140C>T
  hgvsp: ENSP00000385557.1:p.Ala47Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.79C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.310C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.140C>T
  hgvsp: ENSP00000400795.2:p.Ala47Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.149C>T
  hgvsp: ENSP00000368691.3:p.Ala50Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.174C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.140C>T
  hgvsp: ENSP00000385321.3:p.Ala47Val
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37746
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala47Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-32168381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168381
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168381
    reference: chr 2
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.167A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.133A>G
  hgvsp: ENSP00000385321.3:p.Ile45Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.133A>G
  hgvsp: ENSP00000400795.2:p.Ile45Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.133A>G
  hgvsp: ENSP00000385557.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.133A>G
  hgvsp: ENSP00000295065.4:p.Ile45Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.206A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.303A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.72A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.142A>G
  hgvsp: ENSP00000368691.3:p.Ile48Val
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37747
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile45Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-32168389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168389
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168389
    reference: chr 2
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.295C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.64C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.159C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.125C>T
  hgvsp: ENSP00000385557.1:p.Ala42Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.134C>T
  hgvsp: ENSP00000368691.3:p.Ala45Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.125C>T
  hgvsp: ENSP00000400795.2:p.Ala42Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.125C>T
  hgvsp: ENSP00000385321.3:p.Ala42Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.125C>T
  hgvsp: ENSP00000295065.4:p.Ala42Val
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.198C>T
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala42Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-32168402-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168402
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168402
    reference: chr 2
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.282A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.121A>T
  hgvsp: ENSP00000368691.3:p.Thr41Ser
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.146A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.112A>T
  hgvsp: ENSP00000385321.3:p.Thr38Ser
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.112A>T
  hgvsp: ENSP00000385557.1:p.Thr38Ser
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.185A>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.112A>T
  hgvsp: ENSP00000400795.2:p.Thr38Ser
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.51A>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.112A>T
  hgvsp: ENSP00000295065.4:p.Thr38Ser
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr38Ser
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: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-32168425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168425
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168425
    reference: chr 2
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.28G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.98G>A
  hgvsp: ENSP00000368691.3:p.Gly33Asp
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.259G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.89G>A
  hgvsp: ENSP00000400795.2:p.Gly30Asp
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.89G>A
  hgvsp: ENSP00000385557.1:p.Gly30Asp
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.89G>A
  hgvsp: ENSP00000295065.4:p.Gly30Asp
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.89G>A
  hgvsp: ENSP00000385321.3:p.Gly30Asp
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.162G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.123G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6523
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly30Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

2-32168430-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168430
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168430
    reference: chr 2
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.157A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.84A>G
  hgvsp: ENST00000426310.2:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.254A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.23A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.84A>G
  hgvsp: ENST00000404530.1:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.93A>G
  hgvsp: ENST00000379383.3:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.84A>G
  hgvsp: ENST00000295065.5:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.84A>G
  hgvsp: ENST00000407893.3:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.118A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu28Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

2-32168439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168439
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168439
    reference: chr 2
allele count: 2
allele frequency: 1.648913366091746e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.245T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.109T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.75T>C
  hgvsp: ENST00000426310.2:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.75T>C
  hgvsp: ENST00000404530.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.84T>C
  hgvsp: ENST00000379383.3:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.75T>C
  hgvsp: ENST00000295065.5:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.14T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.148T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.75T>C
  hgvsp: ENST00000407893.3:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn25Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-32168442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168442
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168442
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.72G>A
  hgvsp: ENST00000407893.3:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.72G>A
  hgvsp: ENST00000426310.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.106G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.242G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.11G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.81G>A
  hgvsp: ENST00000379383.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.72G>A
  hgvsp: ENST00000295065.5:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.145G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.72G>A
  hgvsp: ENST00000404530.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu24Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-32168448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168448
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168448
    reference: chr 2
allele count: 9
allele frequency: 7.41962077493817e-5
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.66G>A
  hgvsp: ENST00000404530.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000422936
  gene symbol: MEMO1
  hgvsc: ENST00000422936.1:n.5G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.66G>A
  hgvsp: ENST00000407893.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.139G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.66G>A
  hgvsp: ENST00000426310.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.236G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.100G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.66G>A
  hgvsp: ENST00000295065.5:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.75G>A
  hgvsp: ENST00000379383.3:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro22Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-32168456-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168456
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168456
    reference: chr 2
allele count: 38
allele frequency: 3.132883737035633e-4
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-4A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-4A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-4A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6444
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.62-4A>G
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

2-32168462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168462
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168462
    reference: chr 2
allele count: 2
allele frequency: 1.648858989579211e-5
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-10C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-10C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-10C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

2-32168462-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168462
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168462
    reference: chr 2
allele count: 437
allele frequency: 3.602756892230576e-3
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-10C>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-10C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-10C>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 9.75e1
  variant carriers: 320
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-32168478-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168478
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168477
    reference: chr 2
allele count: 2
allele frequency: 1.648804616652927e-5
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-27delT
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-27delT
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-27delT
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37760
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GA
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

2-32168480-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168480
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168479
    reference: chr 2
allele count: 2
allele frequency: 1.648940555692967e-5
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-29delA
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-29delA
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-29delA
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3058
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37760
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: GT
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

2-32168483-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168483
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168483
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-31T>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-31T>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-31T>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

2-32168493-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168493
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168493
    reference: chr 2
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-41A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-41A>G
  variant of: http://identifiers.org/hgnc/24590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5704
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

2-32168498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168498
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168498
    reference: chr 2
allele count: 2
allele frequency: 1.649892756970797e-5
allele num: 121220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-46A>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-46A>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-46A>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37750
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

2-32168502-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32168502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32168502
    reference: chr 2
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.71-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-50C>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-50C>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-50C>A
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

2-32188237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32188237
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32188237
    reference: chr 2
allele count: 2
allele frequency: 1.473839351510685e-4
allele num: 13570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-19785C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.70+4C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-19785C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-19785C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-19785C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-19785C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-19785C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-19785C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
hgvs: c.70+4C>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

2-32188239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32188239
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32188239
    reference: chr 2
allele count: 142
allele frequency: 1.016027475672582e-2
allele num: 13976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.70+2T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-19787T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-19787T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-19787T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-19787T>C
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-19787T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-19787T>C
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-19787T>C
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 9.75e1
  variant carriers: 128
hgvs: c.70+2T>C
num of homozygotes: 3
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

2-32188241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32188241
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32188241
    reference: chr 2
allele count: 179
allele frequency: 1.254907459338194e-2
allele num: 14264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-19789G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-19789G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.70G>A
  hgvsp: ENSP00000368691.3:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-19789G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-19789G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-19789G>A
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-19789G>A
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-19789G>A
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 9.75e1
  variant carriers: 163
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Gly24Arg
num of homozygotes: 4
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

2-32188242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32188242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32188242
    reference: chr 2
allele count: 1
allele frequency: 6.930006930006929e-5
allele num: 14430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.69C>T
  hgvsp: ENST00000379383.3:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-19790C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-19790C>T
  variant of: http://identifiers.org/hgnc/24590
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
hgvs: c.69C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/2-32188347-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32188347
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32188347
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 11192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.232-19895T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.62-19895T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.135-19895T>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.96-19895T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.62-19895T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000368691
  ensembl transcript: ENST00000379383
  gene symbol: MEMO1
  hgvsc: ENST00000379383.3:c.-37T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.62-19895T>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.62-19895T>G
  variant of: http://identifiers.org/hgnc/14014
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

2-32235223-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32235223
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32235223
    reference: chr 2
allele count: 1
allele frequency: 1.01667344448963e-4
allele num: 9836
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.231+33C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.61+33C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.134+13268C>G
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.61+33C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.61+33C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.61+33C>G
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.95+788C>G
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4149
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19491
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

2-32235224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32235224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32235224
    reference: chr 2
allele count: 4
allele frequency: 4.001600640256103e-4
allele num: 9996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.61+32C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.61+32C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.61+32C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.61+32C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.231+32C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.134+13267C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.95+787C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19708
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-32235238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32235238
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 32235238
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 12876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000490459
  gene symbol: MEMO1
  hgvsc: ENST00000490459.1:n.95+773C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162961
  ensembl transcript: ENST00000446765
  gene symbol: DPY30
  hgvsc: ENST00000446765.1:n.134+13253C>T
  variant of: http://identifiers.org/hgnc/24590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl transcript: ENST00000413686
  gene symbol: MEMO1
  hgvsc: ENST00000413686.1:n.231+18C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000295065
  ensembl transcript: ENST00000295065
  gene symbol: MEMO1
  hgvsc: ENST00000295065.5:c.61+18C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385321
  ensembl transcript: ENST00000407893
  gene symbol: MEMO1
  hgvsc: ENST00000407893.3:c.61+18C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000400795
  ensembl transcript: ENST00000426310
  gene symbol: MEMO1
  hgvsc: ENST00000426310.2:c.61+18C>T
  variant of: http://identifiers.org/hgnc/14014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162959
  ensembl protein: ENSP00000385557
  ensembl transcript: ENST00000404530
  gene symbol: MEMO1
  hgvsc: ENST00000404530.1:c.61+18C>T
  variant of: http://identifiers.org/hgnc/14014
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30136
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28133
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Other
reference allele: G

GenotypeQuality
all individuals: 121
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.02757502027575e-4
allele num: 4932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.52e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

FS
type: SiteQuality
SIO_000300: 1.0523e1

DP
type: SiteQuality
SIO_000300: 2.65006e5

VQSLOD
type: SiteQuality
SIO_000300: -5.472e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.458e0

QD
type: SiteQuality
SIO_000300: 1.016e1

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 9.75e1
variant carriers: 8

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

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

GenotypeQuality
all individuals: 738
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.17820324005891e-3
allele num: 6790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

DP
type: SiteQuality
SIO_000300: 2.69931e5

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 1.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.455180442374854e-4
allele num: 6872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.73182e5

QD
type: SiteQuality
SIO_000300: 1.173e1

VQSLOD
type: SiteQuality
SIO_000300: -1.587e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.859e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-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: 41
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5170
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.357220412595005e-4
allele num: 7368
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

DP
type: SiteQuality
SIO_000300: 2.87204e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 421
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GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.326611833377554e-4
allele num: 7538
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 2.89816e5

FS
type: SiteQuality
SIO_000300: 4.492e0

MQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
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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
all individuals: 428
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GenotypeQuality
all individuals: 1737
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5256
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.956739646531258e-4
allele num: 7582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: -1.375e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.537e0

QD
type: SiteQuality
SIO_000300: 6.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

FS
type: SiteQuality
SIO_000300: 3.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 2.9086e5

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 13
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.318565400843882e-4
allele num: 7584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.90878e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.166e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.087e0

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 23

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 3.378378378378379e-3
allele num: 7104
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5066
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.76123e5

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: 11

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
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allele frequency: 4.644681839294008e-4
allele num: 8612
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.051619494020792e-4
allele num: 66564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

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

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.007810153199159e-5
allele num: 66580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.28e-1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.003634397621121e-5
allele num: 66586
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

ClippingRankSum
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SIO_000300: 1.06e0

ReadPosRankSum
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MQ
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SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.978492e6

BaseQRankSum
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SIO_000300: 8.47e-1

QD
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VQSLOD
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SIO_000300: -3.979e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

South Asian
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allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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SIO_000300: 6.860000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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QD
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SIO_000300: 1.432e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

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

South Asian
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allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

DP
type: SiteQuality
SIO_000300: 1.985095e6

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
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SIO_000300: 1.235e1

BaseQRankSum
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SIO_000300: 2.54e0

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.508e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.818e0

DP
type: SiteQuality
SIO_000300: 1.985839e6

QD
type: SiteQuality
SIO_000300: 1.393e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.211827435773146e-3
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 1
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allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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DP
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MQ
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QD
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SIO_000300: 1.383e1

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 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 frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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allele num: 16502
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East Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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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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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

Latino
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num of homozygotes: 0

East Asian
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South Asian
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allele num: 16504
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European (Non-Finnish)
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Other
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

European (Finnish)
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African
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allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

South Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

DP
type: SiteQuality
SIO_000300: 1.988484e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 5.492e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.039e1

QD
type: SiteQuality
SIO_000300: 1.2e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

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

GenotypeQuality
all individuals: 36
bin: 3.25e1
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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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
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GenotypeQuality
all individuals: 1424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6641
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 9014
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33264
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

QD
type: SiteQuality
SIO_000300: 1.531e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 6.352e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 1.989897e6

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 6640
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1030
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.359999999999999e-2

QD
type: SiteQuality
SIO_000300: 3.19e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.989851e6

GenotypeQuality
all individuals: 1418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
all individuals: 9008
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variant carriers: 0

GenotypeQuality
all individuals: 6661
bin: 9.75e1
variant carriers: 56

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.93050193050193e-4
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 7.799376049916006e-4
allele num: 66672
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

DP
type: SiteQuality
SIO_000300: 1.992683e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

FS
type: SiteQuality
SIO_000300: 1.773e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 6615
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2541
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.792400370713623e-4
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

DP
type: SiteQuality
SIO_000300: 1.989622e6

QD
type: SiteQuality
SIO_000300: 1.055e1

MQRankSum
type: SiteQuality
SIO_000300: -4.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.395e0

FS
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

GenotypeQuality
all individuals: 9007
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 177
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -9.01e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

DP
type: SiteQuality
SIO_000300: 1.988986e6

FS
type: SiteQuality
SIO_000300: 1.023e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -9.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

QD
type: SiteQuality
SIO_000300: 1.128e1

FS
type: SiteQuality
SIO_000300: 1.023e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.988986e6

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 8963
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

MQRankSum
type: SiteQuality
SIO_000300: -1.666e0

FS
type: SiteQuality
SIO_000300: 3.118e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.983807e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.048e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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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: 8
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2830
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6602
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505842669557885e-5
allele num: 66408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

QD
type: SiteQuality
SIO_000300: 8.41e0

FS
type: SiteQuality
SIO_000300: 6.443e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.042e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.991e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

DP
type: SiteQuality
SIO_000300: 1.978314e6

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 3.25e1
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GenotypeQuality
all individuals: 8755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6599
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variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 2801
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GenotypeQuality
all individuals: 1026
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GenotypeQuality
all individuals: 1414
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514692517418964e-4
allele num: 6602
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.451000000000001e0

DP
type: SiteQuality
SIO_000300: 1.970017e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
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SIO_000300: 4.89e-1

MQRankSum
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SIO_000300: 1.54e0

BaseQRankSum
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SIO_000300: 5.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

QD
type: SiteQuality
SIO_000300: 2.096e1

VQSLOD
type: SiteQuality
SIO_000300: -1.681e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509570678099149e-5
allele num: 66244
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.3e-3

MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.9617e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ClippingRankSum
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SIO_000300: -3.63e-1

BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 2.059e0

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511350240304688e-5
allele num: 66166
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.442e0

QD
type: SiteQuality
SIO_000300: 1.711e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.950825e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 41
allele frequency: 4.021184778344448e-3
allele num: 10196
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.743375174337517e-4
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.307e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

DP
type: SiteQuality
SIO_000300: 1.913273e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.037298019681691e-5
allele num: 65848
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 1.8185e6

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 3.026e0

QD
type: SiteQuality
SIO_000300: 1.598e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520403819254394e-5
allele num: 65772
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.81169e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.805e1

QD
type: SiteQuality
SIO_000300: 1.652e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.103e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.950248756218905e-5
allele num: 10050
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.504e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.86e-1

FS
type: SiteQuality
SIO_000300: 2.844e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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allele count: 0
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allele num: 8350
num of homozygotes: 0

Latino
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allele frequency: 1.05615208590037e-3
allele num: 11362
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
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Other
type: Population
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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DP
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 1.197604790419162e-4
allele num: 8350
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65056
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.84e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1898
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

FS
type: SiteQuality
SIO_000300: 2.547e0

BaseQRankSum
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SIO_000300: -3.826e0

ReadPosRankSum
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SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.744e0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 2.803641e6

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: 30

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529192280637367e-5
allele num: 65394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.838010047788261e-4
allele num: 16322
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.093764873869586e-3
allele num: 8404
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.815062e6

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

BaseQRankSum
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.087e1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e0

MQ
type: SiteQuality
SIO_000300: 5.738e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 1940
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

African
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allele count: 4
allele frequency: 4.008016032064128e-4
allele num: 9980
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.86e-1

QD
type: SiteQuality
SIO_000300: 6.18e0

VQSLOD
type: SiteQuality
SIO_000300: -8.371e-1

DP
type: SiteQuality
SIO_000300: 2.821903e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 1.4895e1

MQRankSum
type: SiteQuality
SIO_000300: -1.348e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.272e1

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.002004008016032e-4
allele num: 9980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.348e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

DP
type: SiteQuality
SIO_000300: 2.821903e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.86e-1

MQ
type: SiteQuality
SIO_000300: 5.272e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.371e-1

FS
type: SiteQuality
SIO_000300: 1.4895e1

QD
type: SiteQuality
SIO_000300: 6.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 2940
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524436720631727e-5
allele num: 65598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.764e0

QD
type: SiteQuality
SIO_000300: 1.599e1

VQSLOD
type: SiteQuality
SIO_000300: -1.742e0

DP
type: SiteQuality
SIO_000300: 2.821948e6

MQ
type: SiteQuality
SIO_000300: 5.735e1

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.466e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 2.827841e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

FS
type: SiteQuality
SIO_000300: 1.362e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-5
allele num: 66060
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.855e1

VQSLOD
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.832454e6

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.345e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509297271190534e-5
allele num: 66256
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.497e1

VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 3.21e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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South Asian
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African
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European (Non-Finnish)
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Other
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East Asian
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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BaseQRankSum
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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South Asian
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Latino
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European (Non-Finnish)
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allele frequency: 1.503985561738607e-5
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European (Finnish)
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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FS
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DP
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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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African
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South Asian
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Other
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.163061177017911e-4
allele num: 8598
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.499925003749813e-5
allele num: 66670
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South Asian
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African
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Latino
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Other
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East Asian
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DP
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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Other
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European (Non-Finnish)
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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QD
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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MQRankSum
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QD
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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African
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European (Finnish)
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Other
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South Asian
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: 2.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

DP
type: SiteQuality
SIO_000300: 2.845084e6

GenotypeQuality
all individuals: 2881
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 38

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3055
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2974
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

South Asian
type: Population
allele count: 38
allele frequency: 2.302193141887799e-3
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

DP
type: SiteQuality
SIO_000300: 2.845848e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.553e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

MQ
type: SiteQuality
SIO_000300: 5.829e1

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2017
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37817
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3047
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

MQ
type: SiteQuality
SIO_000300: 5.861e1

DP
type: SiteQuality
SIO_000300: 2.869765e6

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

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

GenotypeQuality
all individuals: 2017
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 436

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2879
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variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 173
allele frequency: 2.615663743574237e-2
allele num: 6614
num of homozygotes: 1

Latino
type: Population
allele count: 4
allele frequency: 3.457814661134163e-4
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 248
allele frequency: 3.719256148770246e-3
allele num: 66680
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.702676680146351e-4
allele num: 10386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 2.869765e6

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

MQ
type: SiteQuality
SIO_000300: 5.861e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2023
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 6212
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.043e0

DP
type: SiteQuality
SIO_000300: 2.845247e6

MQRankSum
type: SiteQuality
SIO_000300: -1.88e0

MQ
type: SiteQuality
SIO_000300: 5.54e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

QD
type: SiteQuality
SIO_000300: 4.67e0

FS
type: SiteQuality
SIO_000300: 1.654e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.8e-3

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 6170
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variant carriers: 0

GenotypeQuality
all individuals: 2021
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 2058
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GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.285e0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

QD
type: SiteQuality
SIO_000300: 4.71e0

DP
type: SiteQuality
SIO_000300: 2.84494e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.697e-1

MQ
type: SiteQuality
SIO_000300: 5.53e1

GenotypeQuality
all individuals: 37758
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 71
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GenotypeQuality
all individuals: 2884
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GenotypeQuality
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GenotypeQuality
all individuals: 3230
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GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

FS
type: SiteQuality
SIO_000300: 1.284e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.265e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

VQSLOD
type: SiteQuality
SIO_000300: -2.91e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

DP
type: SiteQuality
SIO_000300: 2.844301e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.923e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

Other
type: Population
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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.447e0

DP
type: SiteQuality
SIO_000300: 2.841315e6

VQSLOD
type: SiteQuality
SIO_000300: -2.548e-1

MQ
type: SiteQuality
SIO_000300: 5.45e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

FS
type: SiteQuality
SIO_000300: 5.54e0

QD
type: SiteQuality
SIO_000300: 1.478e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.742e-1

MQ
type: SiteQuality
SIO_000300: 5.888e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.48e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 2.840284e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.04e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

GenotypeQuality
all individuals: 2056
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variant carriers: 0

GenotypeQuality
all individuals: 37751
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 207
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GenotypeQuality
all individuals: 1985
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 2989
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GenotypeQuality
all individuals: 159
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GenotypeQuality
all individuals: 3057
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.476e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.239e0

DP
type: SiteQuality
SIO_000300: 2.839921e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e0

QD
type: SiteQuality
SIO_000300: 1.343e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.929273084479371e-4
allele num: 5090
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.107e1

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.83425e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 175
bin: 2.5e0
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GenotypeQuality
all individuals: 539
bin: 6.75e1
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GenotypeQuality
all individuals: 92
bin: 4.75e1
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GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.25e1
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GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.881422924901185e-4
allele num: 1012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 60
allele frequency: 1.201923076923077e-2
allele num: 4992
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 3.623188405797101e-3
allele num: 276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 3.631961259079903e-3
allele num: 1652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.681818181818182e-3
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 73
allele frequency: 1.355365763089491e-2
allele num: 5386
num of homozygotes: 2

DP
type: SiteQuality
SIO_000300: 1.87236e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

GenotypeQuality
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2058
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 114
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variant carriers: 3

GenotypeQuality
all individuals: 64
bin: 8.75e1
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GenotypeQuality
all individuals: 266
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1236
bin: 7.5e0
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GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4231
bin: 6.25e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 3.597122302158274e-3
allele num: 278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1652
num of homozygotes: 0

South Asian
type: Population
allele count: 177
allele frequency: 3.129420084865629e-2
allele num: 5656
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.992825827022718e-4
allele num: 5018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.89644e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.909e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
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GenotypeQuality
all individuals: 251
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
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GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1656
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.731301939058172e-4
allele num: 5776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5060
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.793e0

QD
type: SiteQuality
SIO_000300: 6.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

DP
type: SiteQuality
SIO_000300: 1.9098e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.794e-1

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 456
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.543e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.235e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.23912e5

GenotypeQuality
all individuals: 191
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 161
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.560549313358302e-4
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.331e0

DP
type: SiteQuality
SIO_000300: 1.72403e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 4.082e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.58e-2

QD
type: SiteQuality
SIO_000300: 9.31e0

VQSLOD
type: SiteQuality
SIO_000300: -7.904e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

GenotypeQuality
all individuals: 3368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4077
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.152073732718894e-3
allele num: 2604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 9.259259259259259e-3
allele num: 108
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.56e-2

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 4.436e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

DP
type: SiteQuality
SIO_000300: 1.74424e5

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
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GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
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GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0