8-32474395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474395
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474395
    reference: chr 8
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11194C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.494C>T
  hgvsp: ENSP00000384620.2:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.698C>T
  hgvsp: ENSP00000429067.1:p.Thr233Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.130C>T
  hgvsp: ENSP00000432052.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11194C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11194C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.494C>T
  hgvsp: ENSP00000343395.4:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.494C>T
  hgvsp: ENSP00000430120.1:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2313C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.494C>T
  hgvsp: ENSP00000340497.5:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.494C>T
  hgvsp: ENSP00000349275.4:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.494C>T
  hgvsp: ENSP00000287842.3:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.494C>T
  hgvsp: ENSP00000428828.1:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.233C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr165Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

8-32474397-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474397
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474397
    reference: chr 8
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.496T>C
  hgvsp: ENSP00000340497.5:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11196T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.496T>C
  hgvsp: ENSP00000384620.2:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.496T>C
  hgvsp: ENSP00000349275.4:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.700T>C
  hgvsp: ENSP00000429067.1:p.Ser234Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.496T>C
  hgvsp: ENSP00000287842.3:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.496T>C
  hgvsp: ENSP00000428828.1:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2315T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.496T>C
  hgvsp: ENSP00000430120.1:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.235T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11196T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.132T>C
  hgvsp: ENSP00000432052.1:p.Ser45Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.496T>C
  hgvsp: ENSP00000343395.4:p.Ser166Pro
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11196T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser166Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ

8-32474399-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474399
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474399
    reference: chr 8
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.498T>C
  hgvsp: ENST00000338921.4:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.237T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.134T>C
  hgvsp: ENST00000518206.1:c.134T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2317T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.498T>C
  hgvsp: ENST00000405005.3:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.702T>C
  hgvsp: ENST00000523534.1:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.498T>C
  hgvsp: ENST00000356819.4:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.498T>C
  hgvsp: ENST00000287842.3:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.498T>C
  hgvsp: ENST00000521670.1:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.498T>C
  hgvsp: ENST00000523079.1:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11198T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11198T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.498T>C
  hgvsp: ENST00000341377.5:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11198T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser166Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

8-32474408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474408
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474408
    reference: chr 8
allele count: 2
allele frequency: 1.652755970580944e-5
allele num: 121010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11207G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+5G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11207G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11207G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2326G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.502+5G>A
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-32474426-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474426
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474426
    reference: chr 8
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11225T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2344T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11225T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11225T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+23T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+23T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

8-32474433-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474433
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474433
    reference: chr 8
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11232G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11232G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2351G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11232G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-32474444-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474444
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474444
    reference: chr 8
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11243A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2362A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11243A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+41A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11243A>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+41A>C
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-32474449-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474449
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474450
    reference: chr 8
allele count: 270
allele frequency: 2.236024844720497e-3
allele num: 120750
alternate allele: AC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11249dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11249dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+47dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2368dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11249dupC
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+47dupC
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 2
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-32474450-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474450
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474450
    reference: chr 8
allele count: 1
allele frequency: 8.319744417451495e-6
allele num: 120196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11249C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11249C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2368C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+47C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11249C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+47C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

8-32474454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32474454
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32474454
    reference: chr 8
allele count: 2
allele frequency: 1.657522666622466e-5
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+2372C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+11253C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+11253C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+11253C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+51C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+51C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4547
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-32505187-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505187
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505187
    reference: chr 8
allele count: 1
allele frequency: 9.596744784169209e-6
allele num: 104202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+41986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33105C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+41986C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30784C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+41986C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-32505187-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505187
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505187
    reference: chr 8
allele count: 1
allele frequency: 9.596744784169209e-6
allele num: 104202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+41986C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33105C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+41986C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+41986C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30784C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

8-32505188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505188
    reference: chr 8
allele count: 6
allele frequency: 5.754733268113023e-5
allele num: 104262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+41987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+41987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+41987G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33106G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30785G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30785G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

8-32505206-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505206
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505206
    reference: chr 8
allele count: 1
allele frequency: 9.569927459949853e-6
allele num: 104494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42005A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33124A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42005A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42005A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30803A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-32505208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505208
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505208
    reference: chr 8
allele count: 5
allele frequency: 4.785971360747378e-5
allele num: 104472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42007C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42007C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33126C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30805C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42007C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30805C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

8-32505209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505209
    reference: chr 8
allele count: 1
allele frequency: 9.561692037022872e-6
allele num: 104584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42008G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42008G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42008G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30806G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33127G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30806G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

8-32505219-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505219
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505219
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 104922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33137T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42018T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42018T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42018T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30816T>C
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30816T>C
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

8-32505235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505235
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505235
    reference: chr 8
allele count: 1
allele frequency: 9.428625306430323e-6
allele num: 106060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42034C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33153C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42034C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42034C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30832C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30832C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-32505236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505236
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505236
    reference: chr 8
allele count: 3
allele frequency: 2.822679287179391e-5
allele num: 106282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42035G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33154G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42035G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42035G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30833G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

8-32505237-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505237
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505237
    reference: chr 8
allele count: 1
allele frequency: 9.393022862617647e-6
allele num: 106462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33155A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.1A>G
  hgvsp: ENSP00000433289.1:p.Met1?
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42036A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42036A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42036A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30834A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-32505243-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505243
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505243
    reference: chr 8
allele count: 1
allele frequency: 9.325574455386452e-6
allele num: 107232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33161A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.7A>T
  hgvsp: ENSP00000433289.1:p.Ile3Phe
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42042A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42042A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42042A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30840A>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile3Phe
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

8-32505243-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505243
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505243
    reference: chr 8
allele count: 3
allele frequency: 2.797672336615936e-5
allele num: 107232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33161A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42042A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.7A>G
  hgvsp: ENSP00000433289.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42042A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42042A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30840A>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30840A>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile3Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-32505244-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505244
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505244
    reference: chr 8
allele count: 1
allele frequency: 9.314282520817421e-6
allele num: 107362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42043T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.8T>G
  hgvsp: ENSP00000433289.1:p.Ile3Ser
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42043T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30841T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42043T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33162T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30841T>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile3Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

8-32505245-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505245
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505245
    reference: chr 8
allele count: 21
allele frequency: 1.953524716738916e-4
allele num: 107498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42044T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33163T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.9T>G
  hgvsp: ENSP00000433289.1:p.Ile3Met
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42044T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42044T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30842T>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile3Met
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

8-32505247-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505247
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505247
    reference: chr 8
allele count: 1
allele frequency: 9.286430667508636e-6
allele num: 107684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.11A>T
  hgvsp: ENSP00000433289.1:p.Tyr4Phe
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33165A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42046A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42046A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30844A>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42046A>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr4Phe
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-32505252-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505252
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505252
    reference: chr 8
allele count: 5
allele frequency: 4.607021100156639e-5
allele num: 108530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.16C>A
  hgvsp: ENSP00000433289.1:p.Pro6Thr
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33170C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42051C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42051C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30849C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42051C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro6Thr
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-32505252-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505252
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505252
    reference: chr 8
allele count: 8
allele frequency: 7.371233760250621e-5
allele num: 108530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42051C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42051C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33170C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.16C>G
  hgvsp: ENSP00000433289.1:p.Pro6Ala
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42051C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30849C>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro6Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-32505255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505255
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505255
    reference: chr 8
allele count: 8
allele frequency: 7.323190714194174e-5
allele num: 109242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33173G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42054G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42054G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.19G>A
  hgvsp: ENSP00000433289.1:p.Asp7Asn
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30852G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42054G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30852G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11838
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp7Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

8-32505266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505266
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505266
    reference: chr 8
allele count: 4
allele frequency: 3.571237255147045e-5
allele num: 112006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42065G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42065G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42065G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.30G>A
  hgvsp: ENST00000520502.2:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30863G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33184G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30863G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu10Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

8-32505273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505273
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505273
    reference: chr 8
allele count: 2
allele frequency: 1.741492807634705e-5
allele num: 114844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33191G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.37G>A
  hgvsp: ENSP00000433289.1:p.Ala13Thr
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42072G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42072G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30870G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42072G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30870G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala13Thr
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-32505275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505275
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505275
    reference: chr 8
allele count: 4
allele frequency: 3.464403256539061e-5
allele num: 115460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42074C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33193C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.39C>T
  hgvsp: ENST00000520502.2:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42074C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42074C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30872C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21567
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala13Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

6-112408663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112408663
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112408663
    reference: chr 6
allele count: 1
allele frequency: 5.967299200381907e-5
allele num: 16758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000474458
  ensembl transcript: ENST00000605457
  gene symbol: TUBE1
  hgvsc: ENST00000605457.1:c.-26G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000475087
  ensembl transcript: ENST00000604743
  gene symbol: TUBE1
  hgvsc: ENST00000604743.1:c.-26G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603722
  gene symbol: TUBE1
  hgvsc: ENST00000603722.1:n.70G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000368657
  gene symbol: TUBE1
  hgvsc: ENST00000368657.3:n.20G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000474989
  ensembl transcript: ENST00000604967
  gene symbol: TUBE1
  hgvsc: ENST00000604967.1:c.-26G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000357651
  ensembl transcript: ENST00000368662
  gene symbol: TUBE1
  hgvsc: ENST00000368662.5:c.-26G>A
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603621
  gene symbol: TUBE1
  hgvsc: ENST00000603621.1:n.39G>A
  variant of: http://identifiers.org/hgnc/20775
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20938
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

6-112408677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112408677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112408677
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 16052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603621
  gene symbol: TUBE1
  hgvsc: ENST00000603621.1:n.25C>T
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603722
  gene symbol: TUBE1
  hgvsc: ENST00000603722.1:n.56C>T
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000474458
  ensembl transcript: ENST00000605457
  gene symbol: TUBE1
  hgvsc: ENST00000605457.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000357651
  ensembl transcript: ENST00000368662
  gene symbol: TUBE1
  hgvsc: ENST00000368662.5:c.-40C>T
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000475087
  ensembl transcript: ENST00000604743
  gene symbol: TUBE1
  hgvsc: ENST00000604743.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000368657
  gene symbol: TUBE1
  hgvsc: ENST00000368657.3:n.6C>T
  variant of: http://identifiers.org/hgnc/20775
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23272
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8042
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-112408682-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112408682
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112408682
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 15928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000475087
  ensembl transcript: ENST00000604743
  gene symbol: TUBE1
  hgvsc: ENST00000604743.1:c.-45A>C
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000357651
  ensembl transcript: ENST00000368662
  gene symbol: TUBE1
  hgvsc: ENST00000368662.5:c.-45A>C
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000074935
  ensembl protein: ENSP00000474458
  ensembl transcript: ENST00000605457
  gene symbol: TUBE1
  hgvsc: ENST00000605457.1:c.-45A>C
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603722
  gene symbol: TUBE1
  hgvsc: ENST00000603722.1:n.51A>C
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000368657
  gene symbol: TUBE1
  hgvsc: ENST00000368657.3:n.1A>C
  variant of: http://identifiers.org/hgnc/20775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074935
  ensembl transcript: ENST00000603621
  gene symbol: TUBE1
  hgvsc: ENST00000603621.1:n.20A>C
  variant of: http://identifiers.org/hgnc/20775
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23292
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15076
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8411
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

6-112420440-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420440
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420440
    reference: chr 6
allele count: 2
allele frequency: 1.693508780843029e-5
allele num: 118098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-33C>G
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-33C>G
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12475
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13520
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13181
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1969
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3929
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9888
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

8-32505276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505276
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505276
    reference: chr 8
allele count: 1
allele frequency: 8.618906433151761e-6
allele num: 116024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42075G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42075G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42075G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.40G>A
  hgvsp: ENSP00000433289.1:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33194G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30873G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30873G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu14Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-32505281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505281
    reference: chr 8
allele count: 1
allele frequency: 8.542919628212137e-6
allele num: 117056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42080G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33199G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42080G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.45G>A
  hgvsp: ENST00000520502.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42080G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30878G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30878G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg15Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

8-32505283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505283
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505283
    reference: chr 8
allele count: 1
allele frequency: 8.524567804412315e-6
allele num: 117308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.47C>T
  hgvsp: ENSP00000433289.1:p.Ser16Phe
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42082C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42082C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42082C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33201C>T
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30880C>T
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser16Phe
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: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS

8-32505285-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505285
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505285
    reference: chr 8
allele count: 1
allele frequency: 8.523259976475802e-6
allele num: 117326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42084T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.49T>G
  hgvsp: ENSP00000433289.1:p.Ser17Ala
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42084T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33203T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42084T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30882T>G
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser17Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

8-32505289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505289
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505289
    reference: chr 8
allele count: 7
allele frequency: 5.922867344693957e-5
allele num: 118186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42088G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.53G>A
  hgvsp: ENSP00000433289.1:p.Ser18Asn
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33207G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42088G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30886G>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42088G>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser18Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-32505291-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32505291
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 32505291
    reference: chr 8
allele count: 13
allele frequency: 1.097416849569475e-4
allele num: 118460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429067
  ensembl transcript: ENST00000523534
  gene symbol: NRG1
  hgvsc: ENST00000523534.1:c.706+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287842
  ensembl transcript: ENST00000287842
  gene symbol: NRG1
  hgvsc: ENST00000287842.3:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000434640
  ensembl transcript: ENST00000520407
  gene symbol: NRG1
  hgvsc: ENST00000520407.1:c.1045+42090C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000349275
  ensembl transcript: ENST00000356819
  gene symbol: NRG1
  hgvsc: ENST00000356819.4:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000432052
  ensembl transcript: ENST00000518206
  gene symbol: NRG1
  hgvsc: ENST00000518206.1:c.138+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430053
  ensembl transcript: ENST00000518104
  gene symbol: NRG1
  hgvsc: ENST00000518104.1:c.388+33209C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000384620
  ensembl transcript: ENST00000405005
  gene symbol: NRG1
  hgvsc: ENST00000405005.3:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl transcript: ENST00000522569
  gene symbol: NRG1
  hgvsc: ENST00000522569.1:n.241+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000428828
  ensembl transcript: ENST00000521670
  gene symbol: NRG1
  hgvsc: ENST00000521670.1:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000430120
  ensembl transcript: ENST00000523079
  gene symbol: NRG1
  hgvsc: ENST00000523079.1:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000433289
  ensembl transcript: ENST00000520502
  gene symbol: NRG1
  hgvsc: ENST00000520502.2:c.55C>A
  hgvsp: ENSP00000433289.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000343395
  ensembl transcript: ENST00000338921
  gene symbol: NRG1
  hgvsc: ENST00000338921.4:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000340497
  ensembl transcript: ENST00000341377
  gene symbol: NRG1
  hgvsc: ENST00000341377.5:c.502+30888C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000287845
  ensembl transcript: ENST00000287845
  gene symbol: NRG1
  hgvsc: ENST00000287845.5:c.400+42090C>A
  variant of: http://identifiers.org/hgnc/7997
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157168
  ensembl protein: ENSP00000429582
  ensembl transcript: ENST00000519301
  gene symbol: NRG1
  hgvsc: ENST00000519301.1:c.337+42090C>A
  variant of: http://identifiers.org/hgnc/7997
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22172
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro19Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

6-112420442-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420442
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420442
    reference: chr 6
allele count: 1
allele frequency: 8.458662516282926e-6
allele num: 118222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-31A>T
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-31A>T
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12587
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13527
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4779
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6511
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9908
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

6-112420443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420443
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420443
    reference: chr 6
allele count: 1
allele frequency: 8.455515532782033e-6
allele num: 118266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-30G>A
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-30G>A
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13524
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6524
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 880
  num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-112420444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420444
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420444
    reference: chr 6
allele count: 1584
allele frequency: 1.338448278775793e-2
allele num: 118346
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-29G>A
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-29G>A
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 13898
  bin: 2.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 5.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 3.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 4.25e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 12644
  bin: 2.75e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9590
  bin: 3.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6444
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3900
  bin: 8.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15371
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 9.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4687
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 14331
  bin: 9.75e1
  variant carriers: 1425
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 2
num of homozygotes: 109
population: Other
  type: Population
  allele count: 9
  allele frequency: 1.0250569476082e-2
  allele num: 878
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-112420461-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420461
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420461
    reference: chr 6
allele count: 2
allele frequency: 1.67709259228202e-5
allele num: 119254
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-12T>C
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-12T>C
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10023
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20060
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4953
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13516
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11464
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-112420465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420465
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420465
    reference: chr 6
allele count: 64
allele frequency: 5.352960856473737e-4
allele num: 119560
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-8C>T
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-8C>T
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17828
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10086
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13733
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13569
  bin: 9.75e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3041
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3251
  bin: 7.25e1
  variant carriers: 0
hgvs: c.-14-8C>T
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10126
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

6-112420466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420466
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420466
    reference: chr 6
allele count: 12
allele frequency: 1.001418676458316e-4
allele num: 119830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-7G>A
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-7G>A
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 4977
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 4114
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
hgvs: c.-14-7G>A
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8638
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-112420469-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420469
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420469
    reference: chr 6
allele count: 1
allele frequency: 8.321682977165302e-6
allele num: 120168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-14-4C>T
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-14-4C>T
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: c.-14-4C>T
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10260
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-112420478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420478
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420478
    reference: chr 6
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-9C>T
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.503216884132043e-5
  allele num: 66524
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

6-112420479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420479
    reference: chr 6
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-8A>G
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-8A>G
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7072
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 4998
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 2075
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 21923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13535
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8652
  num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

6-112420484-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420484
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420484
    reference: chr 6
allele count: 2
allele frequency: 1.653575857792476e-5
allele num: 120950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.-3A>G
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
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genotype depth: GenotypeDepth
  all individuals: 850
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3058
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7086
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3295
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 13537
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5006
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 902
  num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-112420487-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420487
    reference: chr 6
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.1A>G
  hgvsp: ENSP00000357645.2:p.Met1?
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.1A>G
  hgvsp: ENSP00000474987.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10148
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5007
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 45
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 22131
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  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11540
  num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-112420500-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420500
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420500
    reference: chr 6
allele count: 497
allele frequency: 4.10018644711007e-3
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.14T>G
  hgvsp: ENSP00000357645.2:p.Phe5Cys
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.14T>G
  hgvsp: ENSP00000474987.1:p.Phe5Cys
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 9.75e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 425
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  variant carriers: 23
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
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  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 605
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  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3026
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4095
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 22220
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe5Cys
num of homozygotes: 17
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.073120369245719e-5
  allele num: 16466
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

6-112420506-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420506
    reference: chr 6
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.20C>G
  hgvsp: ENSP00000357645.2:p.Thr7Ser
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.20C>G
  hgvsp: ENSP00000474987.1:p.Thr7Ser
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10205
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5016
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3304
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 24
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 7116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 22345
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr7Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66650
  num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/6-112420507-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420507
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420507
    reference: chr 6
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.21C>A
  hgvsp: ENST00000604268.1:c.21C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.21C>A
  hgvsp: ENST00000368656.2:c.21C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 72
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genotype depth: GenotypeDepth
  all individuals: 290
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genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5018
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 7114
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 3055
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 13516
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 3304
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 16
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genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr7Thr
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10398
  num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-112420515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420515
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420515
    reference: chr 6
allele count: 739
allele frequency: 6.091529559167793e-3
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.29G>A
  hgvsp: ENSP00000474987.1:p.Arg10Lys
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.29G>A
  hgvsp: ENSP00000357645.2:p.Arg10Lys
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 10094
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 5.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.75e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 4.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 14002
  bin: 9.75e1
  variant carriers: 735
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 10
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2048
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genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg10Lys
num of homozygotes: 4
population: Latino
  type: Population
  allele count: 119
  allele frequency: 1.029055690072639e-2
  allele num: 11564
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

6-112420516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420516
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420516
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.30G>A
  hgvsp: ENST00000368656.2:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.30G>A
  hgvsp: ENST00000604268.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 22405
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4130
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genotype quality: GenotypeQuality
  all individuals: 5017
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg10Arg
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.499610101373643e-5
  allele num: 66684
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-112420517-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420517
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420517
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.31A>T
  hgvsp: ENSP00000474987.1:p.Arg11Trp
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.31A>T
  hgvsp: ENSP00000357645.2:p.Arg11Trp
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3067
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg11Trp
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.062075654704171e-5
  allele num: 16496
  num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

6-112420524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420524
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420524
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.38C>T
  hgvsp: ENSP00000357645.2:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.38C>T
  hgvsp: ENSP00000474987.1:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5016
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  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: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 3067
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 4131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro13Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

6-112420547-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420547
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420547
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.61A>G
  hgvsp: ENSP00000357645.2:p.Ile21Val
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.61A>G
  hgvsp: ENSP00000474987.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18493
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7117
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile21Val
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16500
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-112420559-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420559
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420559
    reference: chr 6
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.73C>T
  hgvsp: ENSP00000357645.2:p.Pro25Ser
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.73C>T
  hgvsp: ENSP00000474987.1:p.Pro25Ser
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6251
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 18486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 22412
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5018
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  variant carriers: 0
hgvs: p.Pro25Ser
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 908
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

6-112420571-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420571
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420571
    reference: chr 6
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.85T>C
  hgvsp: ENSP00000474987.1:p.Ser29Pro
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.85T>C
  hgvsp: ENSP00000357645.2:p.Ser29Pro
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
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genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
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genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 217
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genotype depth: GenotypeDepth
  all individuals: 481
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 13518
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3300
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser29Pro
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 2
  allele frequency: 1.212268153715602e-4
  allele num: 16498
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

6-112420577-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420577
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420577
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.91G>T
  hgvsp: ENSP00000474987.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.91G>T
  hgvsp: ENSP00000357645.2:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  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: 7111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22386
  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: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3067
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5011
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala31Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66696
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

6-112420591-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420591
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420591
    reference: chr 6
allele count: 17
allele frequency: 1.401899986805647e-4
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.105G>T
  hgvsp: ENST00000368656.2:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.105G>T
  hgvsp: ENST00000604268.1:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14515
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3067
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 22227
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13531
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly35Gly
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

6-112420598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420598
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420598
    reference: chr 6
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.112A>G
  hgvsp: ENSP00000474987.1:p.Met38Val
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.112A>G
  hgvsp: ENSP00000357645.2:p.Met38Val
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14502
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13519
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 5003
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7091
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met38Val
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8652
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-112420602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420602
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420602
    reference: chr 6
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.116C>T
  hgvsp: ENSP00000474987.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.116C>T
  hgvsp: ENSP00000357645.2:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4127
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser39Leu
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 908
  num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-112420603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420603
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420603
    reference: chr 6
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.117A>G
  hgvsp: ENST00000604268.1:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.117A>G
  hgvsp: ENST00000368656.2:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7080
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13518
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4994
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4126
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser39Ser
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8652
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/6-112420609-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420609
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420609
    reference: chr 6
allele count: 4
allele frequency: 3.306878306878307e-5
allele num: 120960
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.123C>A
  hgvsp: ENST00000368656.2:c.123C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.123C>A
  hgvsp: ENST00000604268.1:c.123C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13520
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4120
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21520
  bin: 6.25e1
  variant carriers: 0
hgvs: c.123C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-112420609-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420609
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420609
    reference: chr 6
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.123C>G
  hgvsp: ENST00000368656.2:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.123C>G
  hgvsp: ENST00000604268.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4120
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21520
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13520
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
hgvs: c.123C>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

6-112420617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112420617
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 112420617
    reference: chr 6
allele count: 2
allele frequency: 1.655546909921693e-5
allele num: 120806
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000357645
  ensembl transcript: ENST00000368656
  gene symbol: FAM229B
  hgvsc: ENST00000368656.2:c.125+6G>A
  variant of: http://identifiers.org/hgnc/33858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203778
  ensembl protein: ENSP00000474987
  ensembl transcript: ENST00000604268
  gene symbol: FAM229B
  hgvsc: ENST00000604268.1:c.125+6G>A
  variant of: http://identifiers.org/hgnc/33858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3283
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4991
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21210
  bin: 6.25e1
  variant carriers: 0
hgvs: c.125+6G>A
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5147
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5092
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3410
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5738
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5603
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40559
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

African
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allele num: 10362
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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VQSLOD
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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DP
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MQ
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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South Asian
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MQ
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FS
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QD
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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South Asian
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Latino
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East Asian
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 266

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

South Asian
type: Population
allele count: 14
allele frequency: 8.509603695599319e-4
allele num: 16452
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.563431700638881e-4
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.13656233607274e-3
allele num: 11438
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.707430340557275e-4
allele num: 10336
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 229
allele frequency: 3.447237693813036e-3
allele num: 66430
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.08e-1

DP
type: SiteQuality
SIO_000300: 3.222046e6

QD
type: SiteQuality
SIO_000300: 1.464e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 3717
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515932450050026e-5
allele num: 65966
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.221711e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.943e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

ReadPosRankSum
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SIO_000300: 1.51e0

MQ
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SIO_000300: 5.945e1

MQRankSum
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SIO_000300: -8.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.094e1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 504
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322340919647004e-4
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.886e1

FS
type: SiteQuality
SIO_000300: 1.6062e1

VQSLOD
type: SiteQuality
SIO_000300: -2.325e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.618e0

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

QD
type: SiteQuality
SIO_000300: 7.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 3.219046e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8894
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.192179303767287e-4
allele num: 8388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.525203e6

FS
type: SiteQuality
SIO_000300: 2.887e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.123e1

MQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.484e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 41
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 70
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.663838141825563e-5
allele num: 60102
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

DP
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MQ
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SIO_000300: 5.925e1

ReadPosRankSum
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SIO_000300: -4.23e-1

MQRankSum
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VQSLOD
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FS
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QD
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SIO_000300: 1.123e1

ClippingRankSum
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SIO_000300: -1.82e-1

BaseQRankSum
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SIO_000300: -1.484e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.663008048958957e-5
allele num: 60132
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.420866489832007e-4
allele num: 11310
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 1.003e1

DP
type: SiteQuality
SIO_000300: 1.527289e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 941
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GenotypeQuality
all individuals: 271
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele num: 60254
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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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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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African
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 60296
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Other
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Other
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 60874
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Latino
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African
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European (Finnish)
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East Asian
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South Asian
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VQSLOD
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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South Asian
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African
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Latino
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East Asian
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ReadPosRankSum
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MQRankSum
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DP
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FS
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VQSLOD
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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European (Finnish)
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South Asian
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BaseQRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6576
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Other
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African
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allele frequency: 3.477051460361613e-4
allele num: 8628
num of homozygotes: 0

Latino
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South Asian
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East Asian
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.193317422434368e-4
allele num: 8380
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African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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FS
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 3.04228780042592e-4
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.746272050940515e-5
allele num: 61562
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

VQSLOD
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BaseQRankSum
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SIO_000300: -1.59e0

MQRankSum
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.966e1

ClippingRankSum
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SIO_000300: -4.49e-1

FS
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SIO_000300: 0.0e0

QD
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InbreedingCoeff
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SIO_000300: 1.9e-3

DP
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SIO_000300: 1.615985e6

ReadPosRankSum
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SIO_000300: 7.28e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 3
allele frequency: 2.604166666666667e-4
allele num: 11520
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61784
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.935422602089269e-4
allele num: 8424
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -8.49e-1

DP
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VQSLOD
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SIO_000300: 1.43e0

InbreedingCoeff
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SIO_000300: -8.0e-4

BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 5.3e-1

ReadPosRankSum
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SIO_000300: 1.07e0

MQ
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SIO_000300: 5.969e1

MQRankSum
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SIO_000300: 4.59e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 13100
num of homozygotes: 0

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

Latino
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allele count: 4
allele frequency: 3.495892326516343e-4
allele num: 11442
num of homozygotes: 0

Other
type: Population
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

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

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

InbreedingCoeff
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SIO_000300: -1.1e-3

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.1397e1

ClippingRankSum
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SIO_000300: -4.46e-1

MQRankSum
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SIO_000300: 9.76e-1

VQSLOD
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SIO_000300: -1.261e0

DP
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SIO_000300: 1.643555e6

BaseQRankSum
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SIO_000300: -1.29e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.161e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

African
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: 3.142776328608693e-5
allele num: 63638
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
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SIO_000300: 1.384e1

InbreedingCoeff
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SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 3.107e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.671481e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
allele frequency: 6.260760682422915e-5
allele num: 63890
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

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

Other
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BaseQRankSum
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SIO_000300: 2.5e0

ReadPosRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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FS
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ClippingRankSum
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QD
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MQ
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VQSLOD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.596424010217114e-4
allele num: 6264
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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FS
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.703e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 164
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

DP
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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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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Other
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allele num: 162
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -8.599999999999999e-2

QD
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DP
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FS
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VQSLOD
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MQ
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.327668613913967e-4
allele num: 15064
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DP
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QD
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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African
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allele num: 9330
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Latino
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European (Finnish)
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Other
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South Asian
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64628
num of homozygotes: 0

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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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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QD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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Other
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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African
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East Asian
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Other
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Latino
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South Asian
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VQSLOD
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BaseQRankSum
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MQ
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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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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East Asian
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Latino
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15990
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FS
type: SiteQuality
SIO_000300: 1.128e0

QD
type: SiteQuality
SIO_000300: 1.036e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

DP
type: SiteQuality
SIO_000300: 1.711391e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.058e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.751969193068441e-5
allele num: 11426
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.805e0

FS
type: SiteQuality
SIO_000300: 4.929e0

DP
type: SiteQuality
SIO_000300: 1.890689e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: -1.623e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

QD
type: SiteQuality
SIO_000300: 6.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15146
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521421616358325e-5
allele num: 65728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
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FS
type: SiteQuality
SIO_000300: 2.559e0

DP
type: SiteQuality
SIO_000300: 1.894546e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: -2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.908e0

QD
type: SiteQuality
SIO_000300: 1.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.633e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
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Latino
type: Population
allele count: 73
allele frequency: 6.390056022408963e-3
allele num: 11424
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African
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allele count: 1463
allele frequency: 1.468285828984344e-1
allele num: 9964
num of homozygotes: 108

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.170788088937555e-4
allele num: 65754
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.301637612255679e-4
allele num: 15144
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VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.832e0

FS
type: SiteQuality
SIO_000300: 9.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.426e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 1.910154e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.178e-1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024345985180705e-5
allele num: 66130
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: 10086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15458
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.948322e6

VQSLOD
type: SiteQuality
SIO_000300: 9.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.06e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 2.008e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.577e0

South Asian
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allele count: 4
allele frequency: 2.563116749967961e-4
allele num: 15606
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.237136465324385e-3
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num of homozygotes: 0

East Asian
type: Population
allele count: 47
allele frequency: 5.44611819235226e-3
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.509889778046203e-4
allele num: 66230
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

DP
type: SiteQuality
SIO_000300: 1.958479e6

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 1.257e1

FS
type: SiteQuality
SIO_000300: 2.628e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.508523155830442e-4
allele num: 66290
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.821253191907288e-5
allele num: 10182
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.351626016260163e-5
allele num: 15744
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

FS
type: SiteQuality
SIO_000300: 7.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

DP
type: SiteQuality
SIO_000300: 1.962054e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
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: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 4.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 1.96696e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
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: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.94e-2

DP
type: SiteQuality
SIO_000300: 1.97481e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.104e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 3.536e0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

QD
type: SiteQuality
SIO_000300: 1.044e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66534
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: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

QD
type: SiteQuality
SIO_000300: 1.366e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.662e0

MQRankSum
type: SiteQuality
SIO_000300: -7.98e-1

DP
type: SiteQuality
SIO_000300: 1.975242e6

FS
type: SiteQuality
SIO_000300: 3.191e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004627125773691e-5
allele num: 66564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 8.090999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

QD
type: SiteQuality
SIO_000300: 1.354e1

DP
type: SiteQuality
SIO_000300: 1.977715e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: -2.18e0

MQ
type: SiteQuality
SIO_000300: 5.348e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 1.97875e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.454e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

QD
type: SiteQuality
SIO_000300: 1.366e1

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50220608097968e-5
allele num: 66634
num of homozygotes: 0

African
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allele count: 487
allele frequency: 4.687199230028874e-2
allele num: 10390
num of homozygotes: 17

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 5
allele frequency: 4.328254847645429e-4
allele num: 11552
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

QD
type: SiteQuality
SIO_000300: 1.583e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.009974e6

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

Latino
type: Population
allele count: 2
allele frequency: 1.730702665282105e-4
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
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: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.983144e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

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: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.715e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.243e0

MQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

QD
type: SiteQuality
SIO_000300: 1.019e1

DP
type: SiteQuality
SIO_000300: 1.983259e6

African
type: Population
allele count: 23
allele frequency: 2.21026330962906e-3
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 2.11672210462655e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.211453744493392e-2
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 571
allele frequency: 8.563801067850501e-3
allele num: 66676
num of homozygotes: 4

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: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.351e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 2.028006e6

VQSLOD
type: SiteQuality
SIO_000300: 6.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.605e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

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: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 10406
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.851e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-1

FS
type: SiteQuality
SIO_000300: 3.889e0

DP
type: SiteQuality
SIO_000300: 1.986584e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

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: 11566
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: 66688
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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East Asian
type: Population
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allele num: 8654
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MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.214e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.986596e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 3.83e0

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
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South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
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MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 1.986823e6

VQSLOD
type: SiteQuality
SIO_000300: 6.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.043e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 10406
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 6.346e0

VQSLOD
type: SiteQuality
SIO_000300: -4.439e-1

DP
type: SiteQuality
SIO_000300: 1.986962e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

QD
type: SiteQuality
SIO_000300: 1.564e1

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 66704
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.072e1

MQRankSum
type: SiteQuality
SIO_000300: -2.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

DP
type: SiteQuality
SIO_000300: 1.987039e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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: 66698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.52e0

QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.98685e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
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: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 908
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FS
type: SiteQuality
SIO_000300: 5.826e0

VQSLOD
type: SiteQuality
SIO_000300: -1.707e-1

DP
type: SiteQuality
SIO_000300: 1.986601e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 8.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.173e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

Latino
type: Population
allele count: 0
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allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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South Asian
type: Population
allele count: 17
allele frequency: 1.033811724641207e-3
allele num: 16444
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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
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MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

DP
type: SiteQuality
SIO_000300: 1.985791e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.908e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

FS
type: SiteQuality
SIO_000300: 2.066e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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South Asian
type: Population
allele count: 0
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allele num: 16394
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FS
type: SiteQuality
SIO_000300: 2.136e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

QD
type: SiteQuality
SIO_000300: 1.376e1

MQ
type: SiteQuality
SIO_000300: 5.912e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.012e0

MQRankSum
type: SiteQuality
SIO_000300: -2.214e0

DP
type: SiteQuality
SIO_000300: 1.984051e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.09e-1

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.994e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: -1.681e0

DP
type: SiteQuality
SIO_000300: 1.982882e6

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.009e0

QD
type: SiteQuality
SIO_000300: 2.081e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.191e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

African
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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: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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South Asian
type: Population
allele count: 0
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allele num: 16314
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MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 1.982186e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.09e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.006186371963122e-5
allele num: 66598
num of homozygotes: 0

South Asian
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allele count: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
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
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East Asian
type: Population
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: 10402
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.84e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.980047e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.160670280926565e-5
allele num: 16232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.84e0

DP
type: SiteQuality
SIO_000300: 1.980047e6

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

QD
type: SiteQuality
SIO_000300: 9.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3