20-333826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333826
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333826
    reference: chr 20
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3350G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-28G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2144G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-28G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

20-333829-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333829
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333829
    reference: chr 20
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-25T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3353T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2141T>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

20-333833-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333833
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333833
    reference: chr 20
allele count: 7
allele frequency: 5.768438401318501e-5
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2137G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3357G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-21G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-21G>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

20-333834-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333834
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333834
    reference: chr 20
allele count: 4
allele frequency: 3.296196189597204e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2136G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3358G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-20G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-20G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38623
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

20-333836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333836
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333836
    reference: chr 20
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3360C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2134C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-18C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-18C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

20-333838-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333838
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333838
    reference: chr 20
allele count: 7
allele frequency: 5.767772980455489e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3362G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2132G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-16G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-16G>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

20-333844-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333844
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333844
    reference: chr 20
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3368T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-10T>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2126T>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38688
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

20-333848-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333848
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333848
    reference: chr 20
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.190-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2122C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.108-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.190-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.190-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3372C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.190-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.190-6C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.376-6C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: c.190-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

20-333856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333856
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333856
    reference: chr 20
allele count: 305
allele frequency: 2.512397238834247e-3
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.110C>T
  hgvsp: ENST00000608875.1:c.110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.192C>T
  hgvsp: ENST00000382291.3:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2114C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.192C>T
  hgvsp: ENST00000609179.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3380C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.378C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.192C>T
  hgvsp: ENST00000382285.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.192C>T
  hgvsp: ENST00000609504.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.192C>T
  hgvsp: ENST00000470439.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 9.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.192C>T
num of homozygotes: 5
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

20-333861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333861
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333861
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.197T>C
  hgvsp: ENSP00000371722.2:p.Leu66Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.115T>C
  hgvsp: ENSP00000476543.1:p.Leu39Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2109T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.197T>C
  hgvsp: ENSP00000477135.1:p.Leu66Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3385T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.197T>C
  hgvsp: ENSP00000477349.1:p.Leu66Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.197T>C
  hgvsp: ENSP00000371728.3:p.Leu66Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.383T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.197T>C
  hgvsp: ENSP00000476925.1:p.Leu66Pro
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu66Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-333865-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333865
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333865
    reference: chr 20
allele count: 6
allele frequency: 4.942339373970346e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3389C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2105C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.201C>G
  hgvsp: ENST00000609504.1:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.201C>G
  hgvsp: ENST00000382285.2:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.201C>G
  hgvsp: ENST00000470439.1:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.201C>G
  hgvsp: ENST00000609179.1:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.119C>G
  hgvsp: ENST00000608875.1:c.119C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.201C>G
  hgvsp: ENST00000382291.3:c.201C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.387C>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser67Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

20-333867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333867
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333867
    reference: chr 20
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.203C>T
  hgvsp: ENSP00000476925.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.121C>T
  hgvsp: ENSP00000476543.1:p.Ser41Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.203C>T
  hgvsp: ENSP00000477135.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.203C>T
  hgvsp: ENSP00000371728.3:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.389C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.203C>T
  hgvsp: ENSP00000477349.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3391C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.203C>T
  hgvsp: ENSP00000371722.2:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2103C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser68Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

20-333867-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333867
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333866
    reference: chr 20
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.125delG
  hgvsp: ENSP00000476543.1:p.Thr43ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.207delG
  hgvsp: ENSP00000477349.1:p.Thr70ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.207delG
  hgvsp: ENSP00000477135.1:p.Thr70ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.207delG
  hgvsp: ENSP00000371722.2:p.Thr70ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.207delG
  hgvsp: ENSP00000371728.3:p.Thr70ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.207delG
  hgvsp: ENSP00000476925.1:p.Thr70ProfsTer11
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2099delG
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.393delG
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3395delG
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3528
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr70ProfsTer11
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: CG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

20-333868-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333868
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333868
    reference: chr 20
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.122G>A
  hgvsp: ENST00000608875.1:c.122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.390G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2102G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.204G>A
  hgvsp: ENST00000609504.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3392G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.204G>A
  hgvsp: ENST00000470439.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.204G>A
  hgvsp: ENST00000609179.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.204G>A
  hgvsp: ENST00000382291.3:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.204G>A
  hgvsp: ENST00000382285.2:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  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
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser68Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

20-333869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333869
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333869
    reference: chr 20
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.123G>A
  hgvsp: ENSP00000476543.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2101G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.205G>A
  hgvsp: ENSP00000477135.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.205G>A
  hgvsp: ENSP00000477349.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.205G>A
  hgvsp: ENSP00000371722.2:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.205G>A
  hgvsp: ENSP00000371728.3:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.205G>A
  hgvsp: ENSP00000476925.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.391G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3393G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly69Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

20-333869-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333869
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333869
    reference: chr 20
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.205G>C
  hgvsp: ENSP00000371722.2:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.123G>C
  hgvsp: ENSP00000476543.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.391G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.205G>C
  hgvsp: ENSP00000371728.3:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2101G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.205G>C
  hgvsp: ENSP00000477349.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.205G>C
  hgvsp: ENSP00000477135.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.205G>C
  hgvsp: ENSP00000476925.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3393G>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly69Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

20-333870-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333870
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333870
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3394G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.206G>C
  hgvsp: ENSP00000476925.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.206G>C
  hgvsp: ENSP00000477135.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.206G>C
  hgvsp: ENSP00000371722.2:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.206G>C
  hgvsp: ENSP00000477349.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.206G>C
  hgvsp: ENSP00000371728.3:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.392G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2100G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.124G>C
  hgvsp: ENSP00000476543.1:p.Gly42Ala
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly69Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

20-333871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333871
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333871
    reference: chr 20
allele count: 924
allele frequency: 7.610951863200554e-3
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.207G>A
  hgvsp: ENST00000609179.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.207G>A
  hgvsp: ENST00000609504.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.125G>A
  hgvsp: ENST00000608875.1:c.125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.393G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2099G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.207G>A
  hgvsp: ENST00000382285.2:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.207G>A
  hgvsp: ENST00000470439.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3395G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.207G>A
  hgvsp: ENST00000382291.3:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 808
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10107
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly69Gly
num of homozygotes: 4
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

20-333871-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333871
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333871
    reference: chr 20
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.393G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3395G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.207G>T
  hgvsp: ENST00000382291.3:c.207G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.207G>T
  hgvsp: ENST00000609179.1:c.207G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.207G>T
  hgvsp: ENST00000382285.2:c.207G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.207G>T
  hgvsp: ENST00000609504.1:c.207G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.125G>T
  hgvsp: ENST00000608875.1:c.125G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.207G>T
  hgvsp: ENST00000470439.1:c.207G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2099G>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly69Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

20-333875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333875
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333875
    reference: chr 20
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.211C>T
  hgvsp: ENST00000609504.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.211C>T
  hgvsp: ENST00000382291.3:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.397C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.211C>T
  hgvsp: ENST00000382285.2:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.211C>T
  hgvsp: ENST00000470439.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.129C>T
  hgvsp: ENST00000608875.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2095C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3399C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.211C>T
  hgvsp: ENST00000609179.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu71Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

20-333891-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333891
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333891
    reference: chr 20
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.227G>A
  hgvsp: ENSP00000371722.2:p.Gly76Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.145G>A
  hgvsp: ENSP00000476543.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.227G>A
  hgvsp: ENSP00000476925.1:p.Gly76Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.227G>A
  hgvsp: ENSP00000371728.3:p.Gly76Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.227G>A
  hgvsp: ENSP00000477135.1:p.Gly76Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.227G>A
  hgvsp: ENSP00000477349.1:p.Gly76Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3415G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2079G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.413G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly76Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

20-333896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333896
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333896
    reference: chr 20
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.150G>A
  hgvsp: ENSP00000476543.1:p.Ala51Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.232G>A
  hgvsp: ENSP00000477349.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.418G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.232G>A
  hgvsp: ENSP00000371728.3:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.232G>A
  hgvsp: ENSP00000371722.2:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3420G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.232G>A
  hgvsp: ENSP00000477135.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.232G>A
  hgvsp: ENSP00000476925.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2074G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala78Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

20-333898-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333898
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333898
    reference: chr 20
allele count: 247
allele frequency: 2.036743848538822e-3
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.234G>A
  hgvsp: ENST00000609504.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3422G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.234G>A
  hgvsp: ENST00000382291.3:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.152G>A
  hgvsp: ENST00000608875.1:c.152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.234G>A
  hgvsp: ENST00000609179.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.234G>A
  hgvsp: ENST00000470439.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.420G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.234G>A
  hgvsp: ENST00000382285.2:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2072G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala78Ala
num of homozygotes: 2
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-333902-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333902
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333902
    reference: chr 20
allele count: 9
allele frequency: 7.413386929375134e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.424C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.238C>G
  hgvsp: ENSP00000371722.2:p.Leu80Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.238C>G
  hgvsp: ENSP00000476925.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.156C>G
  hgvsp: ENSP00000476543.1:p.Leu53Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.238C>G
  hgvsp: ENSP00000477135.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2068C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3426C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.238C>G
  hgvsp: ENSP00000477349.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.238C>G
  hgvsp: ENSP00000371728.3:p.Leu80Val
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu80Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

20-333909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333909
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333909
    reference: chr 20
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3433C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.245C>T
  hgvsp: ENSP00000371722.2:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.431C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2061C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.245C>T
  hgvsp: ENSP00000476925.1:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.163C>T
  hgvsp: ENSP00000476543.1:p.Thr55Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.245C>T
  hgvsp: ENSP00000477135.1:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.245C>T
  hgvsp: ENSP00000477349.1:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.245C>T
  hgvsp: ENSP00000371728.3:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr82Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

20-333922-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333922
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333923
    reference: chr 20
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3452dupC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.182dupC
  hgvsp: ENSP00000476543.1:p.Lys62GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.264dupC
  hgvsp: ENSP00000371728.3:p.Lys89GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.264dupC
  hgvsp: ENSP00000371722.2:p.Lys89GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.264dupC
  hgvsp: ENSP00000476925.1:p.Lys89GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.450dupC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.264dupC
  hgvsp: ENSP00000477135.1:p.Lys89GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2042dupC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.264dupC
  hgvsp: ENSP00000477349.1:p.Lys89GlnfsTer7
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys89GlnfsTer7
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

20-333930-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333930
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333930
    reference: chr 20
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.452A>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.184A>T
  hgvsp: ENSP00000476543.1:p.Lys62Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2040A>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.266A>T
  hgvsp: ENSP00000477135.1:p.Lys89Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.266A>T
  hgvsp: ENSP00000476925.1:p.Lys89Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.266A>T
  hgvsp: ENSP00000371722.2:p.Lys89Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.266A>T
  hgvsp: ENSP00000371728.3:p.Lys89Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.266A>T
  hgvsp: ENSP00000477349.1:p.Lys89Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3454A>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12545
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys89Met
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

20-333942-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333942
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333942
    reference: chr 20
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.278T>C
  hgvsp: ENSP00000371722.2:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.278T>C
  hgvsp: ENSP00000477135.1:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3466T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.278T>C
  hgvsp: ENSP00000371728.3:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.196T>C
  hgvsp: ENSP00000476543.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.278T>C
  hgvsp: ENSP00000476925.1:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2028T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.464T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.278T>C
  hgvsp: ENSP00000477349.1:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile93Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

20-333943-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333943
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333943
    reference: chr 20
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.279C>T
  hgvsp: ENST00000382291.3:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.279C>T
  hgvsp: ENST00000382285.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.279C>T
  hgvsp: ENST00000609504.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2027C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3467C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.279C>T
  hgvsp: ENST00000470439.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.197C>T
  hgvsp: ENST00000608875.1:c.197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.465C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.279C>T
  hgvsp: ENST00000609179.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile93Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

20-333944-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333944
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333944
    reference: chr 20
allele count: 18
allele frequency: 1.482799525504152e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.198G>A
  hgvsp: ENSP00000476543.1:p.Gly67Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.280G>A
  hgvsp: ENSP00000371722.2:p.Gly94Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.466G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.280G>A
  hgvsp: ENSP00000477135.1:p.Gly94Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.280G>A
  hgvsp: ENSP00000477349.1:p.Gly94Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3468G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.280G>A
  hgvsp: ENSP00000371728.3:p.Gly94Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2026G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.280G>A
  hgvsp: ENSP00000476925.1:p.Gly94Ser
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly94Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

20-333951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333951
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333951
    reference: chr 20
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+1G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.473G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+1G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+1G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.287G>A
  hgvsp: ENSP00000371722.2:p.Gly96Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.287G>A
  hgvsp: ENSP00000371728.3:p.Gly96Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.287G>A
  hgvsp: ENSP00000476925.1:p.Gly96Asp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3475G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2019G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: c.204+1G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

20-333953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333953
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333953
    reference: chr 20
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+3G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+3G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.289G>A
  hgvsp: ENSP00000371722.2:p.Glu97Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.475G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.289G>A
  hgvsp: ENSP00000371728.3:p.Glu97Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.289G>A
  hgvsp: ENSP00000476925.1:p.Glu97Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+3G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3477G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2017G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu97Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

20-333970-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333970
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333970
    reference: chr 20
allele count: 82
allele frequency: 6.755866069074611e-4
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-2000T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+20T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3494T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.306T>C
  hgvsp: ENST00000382291.3:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.306T>C
  hgvsp: ENST00000470439.1:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.492T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+20T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+20T>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.306T>C
  hgvsp: ENST00000382285.2:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39739
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 82
hgvs: p.Asp102Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

20-333971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333971
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333971
    reference: chr 20
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3495C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1999C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.307C>T
  hgvsp: ENSP00000476925.1:p.Gln103Ter
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+21C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.307C>T
  hgvsp: ENSP00000371722.2:p.Gln103Ter
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.493C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+21C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.307C>T
  hgvsp: ENSP00000371728.3:p.Gln103Ter
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+21C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39783
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln103Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

20-333974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333974
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333974
    reference: chr 20
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.310C>T
  hgvsp: ENSP00000476925.1:p.Arg104Trp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.310C>T
  hgvsp: ENSP00000371728.3:p.Arg104Trp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+24C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+24C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1996C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.310C>T
  hgvsp: ENSP00000371722.2:p.Arg104Trp
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+24C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.496C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3498C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg104Trp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

20-333975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333975
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333975
    reference: chr 20
allele count: 4
allele frequency: 3.295598727898891e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.311G>A
  hgvsp: ENSP00000476925.1:p.Arg104Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.311G>A
  hgvsp: ENSP00000371728.3:p.Arg104Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+25G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+25G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.311G>A
  hgvsp: ENSP00000371722.2:p.Arg104Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.497G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3499G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+25G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1995G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg104Gln
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

20-333976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333976
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333976
    reference: chr 20
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3500G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1994G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.312G>A
  hgvsp: ENST00000382291.3:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.312G>A
  hgvsp: ENST00000470439.1:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+26G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.498G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+26G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.312G>A
  hgvsp: ENST00000382285.2:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+26G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg104Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

20-333982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333982
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333982
    reference: chr 20
allele count: 10
allele frequency: 8.238996819747228e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+32C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3506C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.318C>T
  hgvsp: ENST00000470439.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.318C>T
  hgvsp: ENST00000382291.3:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.318C>T
  hgvsp: ENST00000382285.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+32C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1988C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.504C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+32C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala106Ala
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

20-333983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333983
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333983
    reference: chr 20
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+33G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.319G>A
  hgvsp: ENSP00000476925.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3507G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.319G>A
  hgvsp: ENSP00000371728.3:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+33G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+33G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1987G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.319G>A
  hgvsp: ENSP00000371722.2:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.505G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp107Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

20-333995-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 333995
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 333995
    reference: chr 20
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+45G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.331G>T
  hgvsp: ENSP00000371722.2:p.Ala111Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+45G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.517G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3519G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.331G>T
  hgvsp: ENSP00000371728.3:p.Ala111Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.331G>T
  hgvsp: ENSP00000476925.1:p.Ala111Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1975G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+45G>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala111Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

20-334001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334001
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334001
    reference: chr 20
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.337G>A
  hgvsp: ENSP00000371722.2:p.Gly113Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1969G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.337G>A
  hgvsp: ENSP00000371728.3:p.Gly113Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+51G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.523G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+51G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.337G>A
  hgvsp: ENSP00000476925.1:p.Gly113Ser
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+51G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3525G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly113Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

20-334005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334005
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334005
    reference: chr 20
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.527C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.341C>T
  hgvsp: ENSP00000371722.2:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3529C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1965C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.341C>T
  hgvsp: ENSP00000476925.1:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+55C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.341C>T
  hgvsp: ENSP00000371728.3:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+55C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+55C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr114Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

20-334011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334011
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334011
    reference: chr 20
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.286+61G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.347G>A
  hgvsp: ENSP00000371728.3:p.Arg116His
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.347G>A
  hgvsp: ENSP00000371722.2:p.Arg116His
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.347G>A
  hgvsp: ENSP00000476925.1:p.Arg116His
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1959G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3535G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.286+61G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.533G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+61G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg116His
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

20-334017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334017
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334017
    reference: chr 20
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1953C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.353C>T
  hgvsp: ENSP00000371722.2:p.Ala118Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-66C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+67C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.353C>T
  hgvsp: ENSP00000371728.3:p.Ala118Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.353C>T
  hgvsp: ENSP00000476925.1:p.Ala118Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-66C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.539C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3541C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala118Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

20-334026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334026
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334026
    reference: chr 20
allele count: 24
allele frequency: 1.978565539983512e-4
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.548C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3550C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.362C>T
  hgvsp: ENSP00000476925.1:p.Ala121Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.362C>T
  hgvsp: ENSP00000371722.2:p.Ala121Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1944C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-57C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.362C>T
  hgvsp: ENSP00000371728.3:p.Ala121Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-57C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+76C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6530
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala121Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP

20-334027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334027
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334027
    reference: chr 20
allele count: 274
allele frequency: 2.2588995696549e-3
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3551G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.363G>A
  hgvsp: ENST00000382285.2:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.549G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-56G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-56G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.363G>A
  hgvsp: ENST00000470439.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+77G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.363G>A
  hgvsp: ENST00000382291.3:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1943G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7197
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 2340
  bin: 9.75e1
  variant carriers: 266
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala121Ala
num of homozygotes: 8
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/20-334028-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334028
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334028
    reference: chr 20
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.364C>A
  hgvsp: ENSP00000371728.3:p.Leu122Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.364C>A
  hgvsp: ENSP00000371722.2:p.Leu122Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.364C>A
  hgvsp: ENSP00000476925.1:p.Leu122Ile
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3552C>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-55C>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.550C>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+78C>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-55C>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1942C>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu122Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

20-334039-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334039
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334039
    reference: chr 20
allele count: 4
allele frequency: 3.298642608566575e-5
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.375A>G
  hgvsp: ENST00000470439.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.375A>G
  hgvsp: ENST00000382285.2:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-44A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.375A>G
  hgvsp: ENST00000382291.3:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1931A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.561A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3563A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+89A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-44A>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala125Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

20-334040-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334040
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334040
    reference: chr 20
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.562G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.376G>C
  hgvsp: ENSP00000476925.1:p.Ala126Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1930G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+90G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.376G>C
  hgvsp: ENSP00000371728.3:p.Ala126Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-43G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-43G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3564G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.376G>C
  hgvsp: ENSP00000371722.2:p.Ala126Pro
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala126Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

20-334052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334052
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334052
    reference: chr 20
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.388C>T
  hgvsp: ENSP00000371728.3:p.Leu130Phe
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.388C>T
  hgvsp: ENSP00000476925.1:p.Leu130Phe
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.388C>T
  hgvsp: ENSP00000371722.2:p.Leu130Phe
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3576C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.574C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+102C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-31C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-31C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1918C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9596
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12307
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu130Phe
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

20-334054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334054
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334054
    reference: chr 20
allele count: 3
allele frequency: 2.473655568198684e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-29C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+104C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.390C>T
  hgvsp: ENST00000470439.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.576C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3578C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-29C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1916C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.390C>T
  hgvsp: ENST00000382291.3:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.390C>T
  hgvsp: ENST00000382285.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu130Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

20-334069-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334069
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334069
    reference: chr 20
allele count: 82
allele frequency: 6.759207359293086e-4
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.591C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.405C>G
  hgvsp: ENSP00000476925.1:p.Phe135Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.405C>G
  hgvsp: ENSP00000371722.2:p.Phe135Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1901C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.405C>G
  hgvsp: ENSP00000371728.3:p.Phe135Leu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+119C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3593C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287-14C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287-14C>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10225
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9604
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe135Leu
num of homozygotes: 2
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

20-334083-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334083
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334083
    reference: chr 20
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.287G>T
  hgvsp: ENSP00000477135.1:p.Gly96Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+133G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.419G>T
  hgvsp: ENSP00000371728.3:p.Gly140Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.419G>T
  hgvsp: ENSP00000371722.2:p.Gly140Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.287G>T
  hgvsp: ENSP00000477349.1:p.Gly96Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.419G>T
  hgvsp: ENSP00000476925.1:p.Gly140Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.605G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3607G>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1887G>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly140Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-334107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334107
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334107
    reference: chr 20
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+157C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.443C>T
  hgvsp: ENSP00000476925.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1863C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.629C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.311C>T
  hgvsp: ENSP00000477349.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3631C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.311C>T
  hgvsp: ENSP00000477135.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.443C>T
  hgvsp: ENSP00000371722.2:p.Ala148Val
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.443C>T
  hgvsp: ENSP00000371728.3:p.Ala148Val
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9635
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala148Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-334110-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334110
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334110
    reference: chr 20
allele count: 7
allele frequency: 5.76881871075143e-5
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.314A>C
  hgvsp: ENSP00000477349.1:p.Glu105Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.446A>C
  hgvsp: ENSP00000371728.3:p.Glu149Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+160A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.446A>C
  hgvsp: ENSP00000476925.1:p.Glu149Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3634A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.632A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.314A>C
  hgvsp: ENSP00000477135.1:p.Glu105Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.446A>C
  hgvsp: ENSP00000371722.2:p.Glu149Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1860A>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu149Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

20-334120-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334120
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334120
    reference: chr 20
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1850C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.456C>G
  hgvsp: ENSP00000476925.1:p.Asp152Glu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.324C>G
  hgvsp: ENSP00000477349.1:p.Asp108Glu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.456C>G
  hgvsp: ENSP00000371728.3:p.Asp152Glu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.324C>G
  hgvsp: ENSP00000477135.1:p.Asp108Glu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+170C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3644C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.456C>G
  hgvsp: ENSP00000371722.2:p.Asp152Glu
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.642C>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp152Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-334121-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334121
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334121
    reference: chr 20
allele count: 29
allele frequency: 2.391239816616643e-4
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.643C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3645C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+171C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.325C>G
  hgvsp: ENSP00000477135.1:p.Pro109Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1849C>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.457C>G
  hgvsp: ENSP00000476925.1:p.Pro153Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.457C>G
  hgvsp: ENSP00000371722.2:p.Pro153Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.325C>G
  hgvsp: ENSP00000477349.1:p.Pro109Ala
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.457C>G
  hgvsp: ENSP00000371728.3:p.Pro153Ala
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro153Ala
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

20-334123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334123
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334123
    reference: chr 20
allele count: 3
allele frequency: 2.473941153186436e-5
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.459C>T
  hgvsp: ENST00000470439.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3647C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.327C>T
  hgvsp: ENST00000609179.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+173C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.459C>T
  hgvsp: ENST00000382291.3:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.327C>T
  hgvsp: ENST00000609504.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.459C>T
  hgvsp: ENST00000382285.2:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.645C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1847C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro153Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

20-334124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334124
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334124
    reference: chr 20
allele count: 5
allele frequency: 4.123507290360889e-5
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.460G>A
  hgvsp: ENSP00000476925.1:p.Glu154Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.460G>A
  hgvsp: ENSP00000371728.3:p.Glu154Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.328G>A
  hgvsp: ENSP00000477135.1:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1846G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+174G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.328G>A
  hgvsp: ENSP00000477349.1:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.460G>A
  hgvsp: ENSP00000371722.2:p.Glu154Lys
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3648G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.646G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu154Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

20-334129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334129
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334129
    reference: chr 20
allele count: 8
allele frequency: 6.597502845173102e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.465C>T
  hgvsp: ENST00000470439.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.333C>T
  hgvsp: ENST00000609504.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.651C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.465C>T
  hgvsp: ENST00000382291.3:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.333C>T
  hgvsp: ENST00000609179.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1841C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+179C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3653C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.465C>T
  hgvsp: ENST00000382285.2:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala155Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

20-334130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334130
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334130
    reference: chr 20
allele count: 4
allele frequency: 3.298697014679201e-5
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.334G>A
  hgvsp: ENSP00000477349.1:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.466G>A
  hgvsp: ENSP00000371722.2:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+180G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.466G>A
  hgvsp: ENSP00000476925.1:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477135
  ensembl transcript: ENST00000609179
  gene symbol: NRSN2
  hgvsc: ENST00000609179.1:c.334G>A
  hgvsp: ENSP00000477135.1:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.652G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.466G>A
  hgvsp: ENSP00000371728.3:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3654G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1840G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp156Asn
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

20-334138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334138
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334138
    reference: chr 20
allele count: 3
allele frequency: 2.474063566939913e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.474C>T
  hgvsp: ENST00000382285.2:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.474C>T
  hgvsp: ENST00000382291.3:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.342C>T
  hgvsp: ENST00000609504.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1832C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.474C>T
  hgvsp: ENST00000470439.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3662C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.660C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+188C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His158His
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

20-334139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334139
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334139
    reference: chr 20
allele count: 5
allele frequency: 4.123303260708219e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.475G>A
  hgvsp: ENSP00000476925.1:p.Val159Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1831G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+189G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3663G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.661G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.343G>A
  hgvsp: ENSP00000477349.1:p.Val115Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.475G>A
  hgvsp: ENSP00000371722.2:p.Val159Met
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.475G>A
  hgvsp: ENSP00000371728.3:p.Val159Met
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8705
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val159Met
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

20-334142-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334142
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334142
    reference: chr 20
allele count: 365
allele frequency: 3.010061025894772e-3
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.478G>C
  hgvsp: ENSP00000371728.3:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477349
  ensembl transcript: ENST00000609504
  gene symbol: NRSN2
  hgvsc: ENST00000609504.1:c.346G>C
  hgvsp: ENSP00000477349.1:p.Glu116Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3666G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1828G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+192G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.478G>C
  hgvsp: ENSP00000371722.2:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.664G>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476925
  ensembl transcript: ENST00000470439
  gene symbol: NRSN2
  hgvsc: ENST00000470439.1:c.478G>C
  hgvsp: ENSP00000476925.1:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10212
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 9.75e1
  variant carriers: 359
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu160Gln
num of homozygotes: 6
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

20-334150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334150
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334150
    reference: chr 20
allele count: 3
allele frequency: 2.475165836111019e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.486C>T
  hgvsp: ENST00000382291.3:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1820C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.486C>T
  hgvsp: ENST00000382285.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3674C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.672C>T
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+200C>T
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe162Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

20-334151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334151
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334151
    reference: chr 20
allele count: 10
allele frequency: 8.245790523937529e-5
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.487G>A
  hgvsp: ENSP00000371722.2:p.Gly163Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3675G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.487G>A
  hgvsp: ENSP00000371728.3:p.Gly163Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+201G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.673G>A
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1819G>A
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40958
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly163Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

20-334162-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334162
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334162
    reference: chr 20
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+212A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1808A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.684A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.498A>G
  hgvsp: ENST00000382285.2:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3686A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.498A>G
  hgvsp: ENST00000382291.3:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40968
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12456
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro166Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/20-334167-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334167
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334167
    reference: chr 20
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+217A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.503A>C
  hgvsp: ENSP00000371722.2:p.Gln168Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.689A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.503A>C
  hgvsp: ENSP00000371728.3:p.Gln168Pro
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1803A>C
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3691A>C
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40958
  bin: 6.25e1
  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
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12455
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln168Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

20-334167-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334167
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334167
    reference: chr 20
allele count: 12
allele frequency: 9.895111814763506e-5
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3691A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.503A>G
  hgvsp: ENSP00000371728.3:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+217A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.503A>G
  hgvsp: ENSP00000371722.2:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1803A>G
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.689A>G
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln168Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-334177-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 334177
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 334176
    reference: chr 20
allele count: 3
allele frequency: 2.473859550747106e-5
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371728
  ensembl transcript: ENST00000382291
  gene symbol: NRSN2
  hgvsc: ENST00000382291.3:c.516delC
  hgvsp: ENSP00000371728.3:p.Ile173PhefsTer68
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000492242
  gene symbol: NRSN2
  hgvsc: ENST00000492242.1:n.702delC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl transcript: ENST00000608467
  gene symbol: NRSN2
  hgvsc: ENST00000608467.1:n.334-1790delC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000477183
  ensembl transcript: ENST00000608736
  gene symbol: NRSN2
  hgvsc: ENST00000608736.1:c.189+3704delC
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000371722
  ensembl transcript: ENST00000382285
  gene symbol: NRSN2
  hgvsc: ENST00000382285.2:c.516delC
  hgvsp: ENSP00000371722.2:p.Ile173PhefsTer68
  variant of: http://identifiers.org/hgnc/16229
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125841
  ensembl protein: ENSP00000476543
  ensembl transcript: ENST00000608875
  gene symbol: NRSN2
  hgvsc: ENST00000608875.1:c.204+230delC
  variant of: http://identifiers.org/hgnc/16229
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile173PhefsTer68
num of homozygotes: 0
reference allele: AC

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38552
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.796546e6

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.141e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

FS
type: SiteQuality
SIO_000300: 1.755e0

QD
type: SiteQuality
SIO_000300: 1.146e1

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
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: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.205e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.71e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.796723e6

GenotypeQuality
all individuals: 2392
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3782
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 7
allele frequency: 6.73076923076923e-4
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.871e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.294e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.27e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.797261e6

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997361161089121e-5
allele num: 66696
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 2.797142e6

FS
type: SiteQuality
SIO_000300: 6.919e0

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.977e0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2393
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.951e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

DP
type: SiteQuality
SIO_000300: 2.797151e6

QD
type: SiteQuality
SIO_000300: 1.479e1

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3772
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 38662
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 5.767012687427913e-4
allele num: 10404
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: 6614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.481e0

DP
type: SiteQuality
SIO_000300: 2.797609e6

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

GenotypeQuality
all individuals: 12303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1981
bin: 7.75e1
variant carriers: 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: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.102e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

FS
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.715e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

DP
type: SiteQuality
SIO_000300: 2.797893e6

MQ
type: SiteQuality
SIO_000300: 5.935e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.986e1

VQSLOD
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FS
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SIO_000300: 6.02e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 301
allele frequency: 1.823137492428831e-2
allele num: 16510
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QD
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -3.1e-1

MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10406
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66736
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MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.0e-4

BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.991188635137565e-5
allele num: 66732
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.795292e6

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

European (Non-Finnish)
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allele count: 1
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allele num: 66734
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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Latino
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num of homozygotes: 0

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

East Asian
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African
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 2.997062878379188e-5
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num of homozygotes: 0

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

African
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num of homozygotes: 0

European (Finnish)
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Other
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.749e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.43e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

DP
type: SiteQuality
SIO_000300: 2.795114e6

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeQuality
all individuals: 12354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 382
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 6614
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.779e0

FS
type: SiteQuality
SIO_000300: 1.835e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 2.794489e6

QD
type: SiteQuality
SIO_000300: 1.136e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

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

GenotypeQuality
all individuals: 38935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3605
bin: 9.75e1
variant carriers: 920

Latino
type: Population
allele count: 38
allele frequency: 3.283221012614481e-3
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 26
allele frequency: 2.498558523928503e-3
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 56
allele frequency: 3.391472868217054e-3
allele num: 16512
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 779
allele frequency: 1.167286022536562e-2
allele num: 66736
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.023888720895071e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.506607929515419e-3
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.491e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.287e1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

DP
type: SiteQuality
SIO_000300: 2.865337e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38935
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 366
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12349
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variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 837
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
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: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

DP
type: SiteQuality
SIO_000300: 2.865337e6

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.491e0

QD
type: SiteQuality
SIO_000300: 1.287e1

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 244
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 39525
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variant carriers: 0

GenotypeQuality
all individuals: 12512
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 375
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GenotypeQuality
all individuals: 2413
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 2.768634e6

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.304e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.113e0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 12496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
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variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

FS
type: SiteQuality
SIO_000300: 4.696e0

QD
type: SiteQuality
SIO_000300: 1.42e1

DP
type: SiteQuality
SIO_000300: 2.7686e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.343e0

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.93e-1

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2738
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.768599e6

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.962e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.157e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2409
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 848
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 2008
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 245

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

Latino
type: Population
allele count: 9
allele frequency: 7.776049766718507e-4
allele num: 11574
num of homozygotes: 1

East Asian
type: Population
allele count: 49
allele frequency: 5.664739884393063e-3
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
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: 158
allele frequency: 1.520107754473735e-2
allele num: 10394
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.817080557238038e-3
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.788138e6

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 849
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2022
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 39701
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 376
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GenotypeQuality
all individuals: 2476
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 12538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.04890913450012e-4
allele num: 66736
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.62e-1

FS
type: SiteQuality
SIO_000300: 3.366e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

MQRankSum
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SIO_000300: 7.92e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
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 frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.99895036737142e-5
allele num: 66690
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.447e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.936e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.138e0

DP
type: SiteQuality
SIO_000300: 2.758789e6

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

Latino
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allele num: 11574
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6612
num of homozygotes: 0

South Asian
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

Latino
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African
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66726
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African
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European (Finnish)
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South Asian
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East Asian
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Latino
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Other
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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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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South Asian
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European (Finnish)
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Other
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Latino
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East Asian
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African
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European (Non-Finnish)
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MQRankSum
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FS
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 2.758077e6

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.455e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

South Asian
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allele count: 82
allele frequency: 4.96608527131783e-3
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

QD
type: SiteQuality
SIO_000300: 1.437e1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

DP
type: SiteQuality
SIO_000300: 2.760136e6

FS
type: SiteQuality
SIO_000300: 5.55e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
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: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.253e0

VQSLOD
type: SiteQuality
SIO_000300: -1.846e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 1.3896e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.756195e6

GenotypeQuality
all individuals: 2
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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

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49667246237784e-5
allele num: 66716
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.323e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.33e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

DP
type: SiteQuality
SIO_000300: 2.756036e6

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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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.299e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 1.146e0

QD
type: SiteQuality
SIO_000300: 1.221e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 2.755926e6

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.213e0

VQSLOD
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0914e1

BaseQRankSum
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SIO_000300: -3.252e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.87e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 10

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498935755613514e-4
allele num: 66714
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: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.194e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
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allele num: 10404
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
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variant carriers: 2

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

Other
type: Population
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.887e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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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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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 4.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 2.751932e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.751353e6

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.871e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.505e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

QD
type: SiteQuality
SIO_000300: 1.235e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.035e0

FS
type: SiteQuality
SIO_000300: 1.586e0

DP
type: SiteQuality
SIO_000300: 2.750521e6

QD
type: SiteQuality
SIO_000300: 9.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.083e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.371e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
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: 5.933e1

FS
type: SiteQuality
SIO_000300: 3.671e0

QD
type: SiteQuality
SIO_000300: 1.041e1

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

DP
type: SiteQuality
SIO_000300: 2.749405e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.149842507874606e-4
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
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: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.366e1

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 2.494e0

DP
type: SiteQuality
SIO_000300: 2.746996e6

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 154
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GenotypeQuality
all individuals: 120
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variant carriers: 0

African
type: Population
allele count: 260
allele frequency: 2.501924557351809e-2
allele num: 10392
num of homozygotes: 8

Latino
type: Population
allele count: 10
allele frequency: 8.640055296353896e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000060000600006e-5
allele num: 66666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.747176e6

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

FS
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.775e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.004e0

DP
type: SiteQuality
SIO_000300: 2.741798e6

VQSLOD
type: SiteQuality
SIO_000300: -1.942e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 757
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

African
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: 904
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

FS
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 231
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 210
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
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European (Non-Finnish)
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allele frequency: 4.501665616278023e-5
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African
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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Other
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Latino
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European (Finnish)
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East Asian
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FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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African
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South Asian
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allele frequency: 4.96608527131783e-3
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Latino
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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ReadPosRankSum
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QD
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FS
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MQ
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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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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Latino
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European (Non-Finnish)
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East Asian
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African
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South Asian
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European (Finnish)
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MQ
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QD
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DP
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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Other
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East Asian
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South Asian
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DP
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FS
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MQ
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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Latino
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East Asian
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DP
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MQRankSum
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MQ
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QD
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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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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East Asian
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
type: SiteQuality
SIO_000300: 2.738567e6

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 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: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

DP
type: SiteQuality
SIO_000300: 2.73716e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.679e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 2.057e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.323e0

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 2299
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

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

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

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: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 3.584e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.73704e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.417e1

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

GenotypeQuality
all individuals: 12411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 9.75e1
variant carriers: 8

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: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.200948749512115e-4
allele num: 66614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.345e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

FS
type: SiteQuality
SIO_000300: 1.185e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

DP
type: SiteQuality
SIO_000300: 2.737583e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
all individuals: 40702
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 11576
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.890173410404624e-4
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.737197e6

FS
type: SiteQuality
SIO_000300: 5.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 746
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1934
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variant carriers: 3

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 2302
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926782273603083e-4
allele num: 10380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.73748e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.122e0

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12412
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variant carriers: 0

GenotypeQuality
all individuals: 2302
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 1933
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variant carriers: 5

GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 2
allele frequency: 1.926782273603083e-4
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
SIO_000300: 1.482e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 4.175e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

DP
type: SiteQuality
SIO_000300: 2.737805e6

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

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

GenotypeQuality
all individuals: 2287
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2
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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: 40709
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 12388
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 342
allele frequency: 3.296703296703297e-2
allele num: 10374
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.006304413089163e-5
allele num: 66620
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.295560545862843e-3
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

DP
type: SiteQuality
SIO_000300: 2.760868e6

QD
type: SiteQuality
SIO_000300: 1.512e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12456
bin: 6.75e1
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: 197
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variant carriers: 0

GenotypeQuality
all individuals: 749
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
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: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.328e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 2.735838e6

MQRankSum
type: SiteQuality
SIO_000300: -6.43e-1

FS
type: SiteQuality
SIO_000300: 4.264e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.176e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 195
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GenotypeQuality
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GenotypeQuality
all individuals: 292
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.927153594141453e-4
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502476361999099e-5
allele num: 66630
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: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 2.736418e6

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.319e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.74e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.937e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.735254e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 5.159e0

QD
type: SiteQuality
SIO_000300: 1.341e1

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 10382
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.183e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.735706e6

QD
type: SiteQuality
SIO_000300: 1.223e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 12455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40958
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1702
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 747
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.267441860465116e-4
allele num: 16512
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.735706e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.183e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.223e1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40949
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 7.25e1
variant carriers: 0