http://identifiers.org/exac.variant/1-163042640-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042640
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042640
    reference: chr 1
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.141C>A
  hgvsp: ENSP00000356882.3:p.Asn47Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.508C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.195C>A
  hgvsp: ENSP00000356884.4:p.Asn65Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.334C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.486C>A
  hgvsp: ENSP00000397181.2:p.Asn162Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.141C>A
  hgvsp: ENSP00000432194.1:p.Asn47Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.141C>A
  hgvsp: ENSP00000433261.1:p.Asn47Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.195C>A
  hgvsp: ENSP00000436106.1:p.Asn65Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.195C>A
  hgvsp: ENSP00000356885.6:p.Asn65Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.622C>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn162Lys
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

1-163042653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042653
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042653
    reference: chr 1
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.154G>A
  hgvsp: ENSP00000356882.3:p.Glu52Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.208G>A
  hgvsp: ENSP00000356884.4:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.499G>A
  hgvsp: ENSP00000397181.2:p.Glu167Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.635G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.521G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.208G>A
  hgvsp: ENSP00000356885.6:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.208G>A
  hgvsp: ENSP00000436106.1:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.154G>A
  hgvsp: ENSP00000432194.1:p.Glu52Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.154G>A
  hgvsp: ENSP00000433261.1:p.Glu52Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.347G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu167Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/1-163042654-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042654
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042654
    reference: chr 1
allele count: 2
allele frequency: 1.6627315353663e-5
allele num: 120284
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.500A>C
  hgvsp: ENSP00000397181.2:p.Glu167Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.522A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.209A>C
  hgvsp: ENSP00000356884.4:p.Glu70Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.155A>C
  hgvsp: ENSP00000433261.1:p.Glu52Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.209A>C
  hgvsp: ENSP00000356885.6:p.Glu70Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.209A>C
  hgvsp: ENSP00000436106.1:p.Glu70Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.155A>C
  hgvsp: ENSP00000432194.1:p.Glu52Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.155A>C
  hgvsp: ENSP00000356882.3:p.Glu52Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.636A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.348A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu167Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-163042656-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042656
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042656
    reference: chr 1
allele count: 1
allele frequency: 8.317391665973551e-6
allele num: 120230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211T>C
  hgvsp: ENSP00000436106.1:p.Cys71Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211T>C
  hgvsp: ENSP00000356885.6:p.Cys71Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157T>C
  hgvsp: ENSP00000356882.3:p.Cys53Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157T>C
  hgvsp: ENSP00000433261.1:p.Cys53Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157T>C
  hgvsp: ENSP00000432194.1:p.Cys53Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502T>C
  hgvsp: ENSP00000397181.2:p.Cys168Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211T>C
  hgvsp: ENSP00000356884.4:p.Cys71Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys168Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

1-163042669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042669
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042669
    reference: chr 1
allele count: 1
allele frequency: 8.34306691139663e-6
allele num: 119860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+13G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+13G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33885
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

1-163042676-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042676
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042676
    reference: chr 1
allele count: 1
allele frequency: 8.358967500334358e-6
allele num: 119632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+20G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+20G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-163042676-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042676
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042676
    reference: chr 1
allele count: 1
allele frequency: 8.358967500334358e-6
allele num: 119632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+20G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+20G>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13782
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

1-163042680-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042680
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042680
    reference: chr 1
allele count: 5
allele frequency: 4.182420450363034e-5
allele num: 119548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+24T>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+24T>G
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30273
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4608
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-163042686-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042686
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042686
    reference: chr 1
allele count: 1
allele frequency: 8.379139294811638e-6
allele num: 119344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+30A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+30A>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

1-163042688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042688
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042688
    reference: chr 1
allele count: 1
allele frequency: 8.37885846432282e-6
allele num: 119348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+32T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+32T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

1-163042694-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042694
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042694
    reference: chr 1
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+38T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+38T>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/1-163042701-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042701
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042701
    reference: chr 1
allele count: 1
allele frequency: 8.426871608184177e-6
allele num: 118668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+45A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+45A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4075
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

1-163042703-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163042703
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163042703
    reference: chr 1
allele count: 1
allele frequency: 8.439530762089629e-6
allele num: 118490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.524+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.157+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.350+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.211+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.211+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.638+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.157+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.502+47T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.157+47T>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23699
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5115
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-163043201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043201
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043201
    reference: chr 1
allele count: 1
allele frequency: 9.02233931213685e-6
allele num: 110836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+545C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-45C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-45C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

1-163043202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043202
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043202
    reference: chr 1
allele count: 1
allele frequency: 9.019409769824663e-6
allele num: 110872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-44C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+546C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-44C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-163043204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043204
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043204
    reference: chr 1
allele count: 1
allele frequency: 9.017620430320846e-6
allele num: 110894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+548A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-42A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-42A>G
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/1-163043218-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043218
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043218
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 111096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+562A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-28A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-28A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40852
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-163043218-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043218
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043218
    reference: chr 1
allele count: 1
allele frequency: 9.001224166486642e-6
allele num: 111096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+562A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-28A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-28A>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-163043220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043220
    reference: chr 1
allele count: 1
allele frequency: 8.998794161582347e-6
allele num: 111126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+564C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-26C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-26C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-163043229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043229
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043229
    reference: chr 1
allele count: 6
allele frequency: 5.384739647838027e-5
allele num: 111426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+573T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-17T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-17T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-163043235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043235
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043235
    reference: chr 1
allele count: 1
allele frequency: 8.962982880702698e-6
allele num: 111570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+579C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-11C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-11C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

1-163043236-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043236
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043236
    reference: chr 1
allele count: 19
allele frequency: 1.701716046286677e-4
allele num: 111652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+580T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-10T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-10T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30006
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 40954
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

1-163043237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043237
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043237
    reference: chr 1
allele count: 2
allele frequency: 1.790542355279414e-5
allele num: 111698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+581G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-9G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-9G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

1-163043243-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043243
    reference: chr 1
allele count: 3
allele frequency: 2.678906291857911e-5
allele num: 111986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-3T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+587T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-3T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6898
  bin: 6.75e1
  variant carriers: 0
hgvs: c.503-3T>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

1-163043245-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043245
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043245
    reference: chr 1
allele count: 2
allele frequency: 1.784057660743595e-5
allele num: 112104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+589G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158-1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212-1G>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
hgvs: c.503-1G>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-163043246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043246
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043246
    reference: chr 1
allele count: 3
allele frequency: 2.674988854213107e-5
allele num: 112150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.212G>A
  hgvsp: ENSP00000436106.1:p.Cys71Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.212G>A
  hgvsp: ENSP00000356885.6:p.Cys71Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.639G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.351G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.158G>A
  hgvsp: ENSP00000433261.1:p.Cys53Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.158G>A
  hgvsp: ENSP00000356882.3:p.Cys53Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.525G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.158G>A
  hgvsp: ENSP00000432194.1:p.Cys53Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.503G>A
  hgvsp: ENSP00000397181.2:p.Cys168Tyr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+590G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys168Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

1-163043254-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043254
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043254
    reference: chr 1
allele count: 1
allele frequency: 8.867606632969762e-6
allele num: 112770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.220G>A
  hgvsp: ENSP00000436106.1:p.Ala74Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.647G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.166G>A
  hgvsp: ENSP00000432194.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.359G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+598G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.220G>A
  hgvsp: ENSP00000356885.6:p.Ala74Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.166G>A
  hgvsp: ENSP00000356882.3:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.533G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.166G>A
  hgvsp: ENSP00000433261.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.511G>A
  hgvsp: ENSP00000397181.2:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala171Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

1-163043257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043257
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043257
    reference: chr 1
allele count: 1
allele frequency: 8.838763280241829e-6
allele num: 113138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.223G>A
  hgvsp: ENSP00000436106.1:p.Ala75Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.650G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.536G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.169G>A
  hgvsp: ENSP00000432194.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.223G>A
  hgvsp: ENSP00000356885.6:p.Ala75Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.169G>A
  hgvsp: ENSP00000356882.3:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.169G>A
  hgvsp: ENSP00000433261.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.514G>A
  hgvsp: ENSP00000397181.2:p.Ala172Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+601G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.362G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6898
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala172Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

1-163043273-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043273
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043273
    reference: chr 1
allele count: 1
allele frequency: 8.688550228508871e-6
allele num: 115094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.378T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.185T>C
  hgvsp: ENSP00000432194.1:p.Leu62Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.185T>C
  hgvsp: ENSP00000356882.3:p.Leu62Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.530T>C
  hgvsp: ENSP00000397181.2:p.Leu177Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.239T>C
  hgvsp: ENSP00000436106.1:p.Leu80Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.666T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+617T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.239T>C
  hgvsp: ENSP00000356885.6:p.Leu80Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.552T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.185T>C
  hgvsp: ENSP00000433261.1:p.Leu62Ser
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu177Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

1-163043277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043277
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043277
    reference: chr 1
allele count: 3
allele frequency: 2.592464569650881e-5
allele num: 115720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+621G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.382G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.189G>A
  hgvsp: ENST00000527809.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.534G>A
  hgvsp: ENST00000421743.2:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.243G>A
  hgvsp: ENST00000367909.6:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.670G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.189G>A
  hgvsp: ENST00000528938.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.243G>A
  hgvsp: ENST00000531057.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.189G>A
  hgvsp: ENST00000367906.3:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000527393
  gene symbol: RGS4
  hgvsc: ENST00000527393.1:n.556G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys178Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-163043299-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043299
    reference: chr 1
allele count: 1
allele frequency: 8.394191219675984e-6
allele num: 119130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.211A>C
  hgvsp: ENSP00000356882.3:p.Ile71Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.692A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.211A>C
  hgvsp: ENSP00000433261.1:p.Ile71Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.265A>C
  hgvsp: ENSP00000436106.1:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.211A>C
  hgvsp: ENSP00000432194.1:p.Ile71Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+643A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.556A>C
  hgvsp: ENSP00000397181.2:p.Ile186Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.265A>C
  hgvsp: ENSP00000356885.6:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.404A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile186Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

1-163043304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043304
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043304
    reference: chr 1
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.270C>T
  hgvsp: ENST00000367909.6:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.561C>T
  hgvsp: ENST00000421743.2:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.216C>T
  hgvsp: ENST00000528938.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.216C>T
  hgvsp: ENST00000367906.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.697C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.409C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.216C>T
  hgvsp: ENST00000527809.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.270C>T
  hgvsp: ENST00000531057.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+648C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3371
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp187Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

1-163043307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043307
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043307
    reference: chr 1
allele count: 2
allele frequency: 1.669978791269351e-5
allele num: 119762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.273C>T
  hgvsp: ENST00000367909.6:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.700C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.219C>T
  hgvsp: ENST00000527809.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.219C>T
  hgvsp: ENST00000528938.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.219C>T
  hgvsp: ENST00000367906.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.273C>T
  hgvsp: ENST00000531057.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.412C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.564C>T
  hgvsp: ENST00000421743.2:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+651C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe188Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

1-163043308-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043308
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043308
    reference: chr 1
allele count: 1
allele frequency: 8.343484572897024e-6
allele num: 119854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.220T>A
  hgvsp: ENSP00000356882.3:p.Trp74Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.413T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.565T>A
  hgvsp: ENSP00000397181.2:p.Trp189Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.220T>A
  hgvsp: ENSP00000432194.1:p.Trp74Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.274T>A
  hgvsp: ENSP00000356885.6:p.Trp92Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.701T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.220T>A
  hgvsp: ENSP00000433261.1:p.Trp74Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+652T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.274T>A
  hgvsp: ENSP00000436106.1:p.Trp92Arg
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp189Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-163043316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043316
    reference: chr 1
allele count: 10
allele frequency: 8.317945134833891e-5
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.709C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.573C>T
  hgvsp: ENST00000421743.2:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.228C>T
  hgvsp: ENST00000527809.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.228C>T
  hgvsp: ENST00000528938.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.421C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.228C>T
  hgvsp: ENST00000367906.3:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.282C>T
  hgvsp: ENST00000367909.6:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+660C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.282C>T
  hgvsp: ENST00000531057.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser191Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ

1-163043330-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043330
    reference: chr 1
allele count: 1
allele frequency: 8.310341388824253e-6
allele num: 120332
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.587A>G
  hgvsp: ENSP00000397181.2:p.Lys196Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.435A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.296A>G
  hgvsp: ENSP00000436106.1:p.Lys99Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.242A>G
  hgvsp: ENSP00000432194.1:p.Lys81Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+674A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.723A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.296A>G
  hgvsp: ENSP00000356885.6:p.Lys99Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.242A>G
  hgvsp: ENSP00000433261.1:p.Lys81Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.242A>G
  hgvsp: ENSP00000356882.3:p.Lys81Arg
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3356
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys196Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-163043332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043332
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043332
    reference: chr 1
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.437A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.244A>G
  hgvsp: ENSP00000356882.3:p.Lys82Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.244A>G
  hgvsp: ENSP00000433261.1:p.Lys82Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.589A>G
  hgvsp: ENSP00000397181.2:p.Lys197Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.725A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.298A>G
  hgvsp: ENSP00000436106.1:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+676A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.244A>G
  hgvsp: ENSP00000432194.1:p.Lys82Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.298A>G
  hgvsp: ENSP00000356885.6:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys197Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/1-163043342-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043342
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043342
    reference: chr 1
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.308C>A
  hgvsp: ENSP00000436106.1:p.Ser103Ter
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.447C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.254C>A
  hgvsp: ENSP00000433261.1:p.Ser85Ter
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.735C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+686C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.599C>A
  hgvsp: ENSP00000397181.2:p.Ser200Ter
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.308C>A
  hgvsp: ENSP00000356885.6:p.Ser103Ter
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.254C>A
  hgvsp: ENSP00000432194.1:p.Ser85Ter
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.254C>A
  hgvsp: ENSP00000356882.3:p.Ser85Ter
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser200Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

1-163043353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043353
    reference: chr 1
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+697C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.265C>T
  hgvsp: ENST00000528938.1:c.265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.265C>T
  hgvsp: ENST00000527809.1:c.265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.319C>T
  hgvsp: ENST00000367909.6:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.265C>T
  hgvsp: ENST00000367906.3:c.265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.610C>T
  hgvsp: ENST00000421743.2:c.610C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.746C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.319C>T
  hgvsp: ENST00000531057.1:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.458C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6933
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu204Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

1-163043365-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043365
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043365
    reference: chr 1
allele count: 1
allele frequency: 8.406752303450132e-6
allele num: 118952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.277G>T
  hgvsp: ENSP00000356882.3:p.Ala93Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.277G>T
  hgvsp: ENSP00000432194.1:p.Ala93Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.758G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.622G>T
  hgvsp: ENSP00000397181.2:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.331G>T
  hgvsp: ENSP00000356885.6:p.Ala111Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+1G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+709G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.470G>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.277G>T
  hgvsp: ENSP00000433261.1:p.Ala93Ser
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3320
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
hgvs: c.330+1G>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-163043372-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043372
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043372
    reference: chr 1
allele count: 2
allele frequency: 1.692076008054282e-5
allele num: 118198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.338A>G
  hgvsp: ENSP00000356885.6:p.Lys113Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.211+716A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.284A>G
  hgvsp: ENSP00000433261.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.477A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+8A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.284A>G
  hgvsp: ENSP00000432194.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.284A>G
  hgvsp: ENSP00000356882.3:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.765A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.629A>G
  hgvsp: ENSP00000397181.2:p.Lys210Arg
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys210Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

1-163043388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043388
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043388
    reference: chr 1
allele count: 1
allele frequency: 8.769160615945842e-6
allele num: 114036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.300C>T
  hgvsp: ENST00000527809.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-723C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.781C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.354C>T
  hgvsp: ENST00000367909.6:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.300C>T
  hgvsp: ENST00000528938.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.645C>T
  hgvsp: ENST00000421743.2:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+24C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.300C>T
  hgvsp: ENST00000367906.3:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.493C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe215Phe
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-163043406-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043406
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043406
    reference: chr 1
allele count: 1
allele frequency: 9.54653937947494e-6
allele num: 104750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-705C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+42C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.318C>A
  hgvsp: ENST00000528938.1:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.511C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.318C>A
  hgvsp: ENST00000367906.3:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.372C>A
  hgvsp: ENST00000367909.6:c.372C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.799C>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.318C>A
  hgvsp: ENST00000527809.1:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.663C>A
  hgvsp: ENST00000421743.2:c.663C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr221Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-163043417-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043417
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043416
    reference: chr 1
allele count: 1
allele frequency: 1.053762987628823e-5
allele num: 94898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+59delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+11delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-688delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+11delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+11delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+11delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.816delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+11delT
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+11delT
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14892
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 7.5e0
  variant carriers: 0
hgvs: c.669+11delT
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: GT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-163043419-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043419
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043419
    reference: chr 1
allele count: 1
allele frequency: 1.074113856068743e-5
allele num: 93100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+55T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+7T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+7T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+7T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+7T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.812T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-692T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+7T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+7T>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13576
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18841
  bin: 6.25e1
  variant carriers: 0
hgvs: c.669+7T>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-163043435-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043435
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043435
    reference: chr 1
allele count: 4
allele frequency: 4.898958971218616e-5
allele num: 81650
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+23A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-676A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+23A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+23A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+23A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+71A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.828A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+23A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+23A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 8167
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

1-163043444-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043444
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043444
    reference: chr 1
allele count: 7
allele frequency: 9.602721685689202e-5
allele num: 72896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+32C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+32C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+80C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.837C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-667C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+32C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+32C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+32C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+32C>G
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16398
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22439
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

1-163043445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043445
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043445
    reference: chr 1
allele count: 2
allele frequency: 2.788855732492958e-5
allele num: 71714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+33G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+33G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+81G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+33G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+33G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+33G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-666G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.838G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+33G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22091
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/1-163043451-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043451
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043451
    reference: chr 1
allele count: 2
allele frequency: 2.994908655286014e-5
allele num: 66780
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-660A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+39A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.844A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+87A>C
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19844
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9333
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-163043462-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163043462
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163043462
    reference: chr 1
allele count: 1
allele frequency: 1.749842514173725e-5
allele num: 57148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.324+50G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.378+50G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.855G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.517+50G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-649G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.324+50G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.330+98G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.669+50G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.324+50G>C
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22494
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16163
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-163044071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044071
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044071
    reference: chr 1
allele count: 1
allele frequency: 8.262004692818665e-6
allele num: 121036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1464G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-40G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-338G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11366
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-163044081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044081
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044081
    reference: chr 1
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1474T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-328T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-30T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-30T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-163044086-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044086
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044086
    reference: chr 1
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-323T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1479T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-25T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-25T>C
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-163044089-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044089
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044089
    reference: chr 1
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1482A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-320A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-22A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-22A>G
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2686
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-163044091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044091
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044091
    reference: chr 1
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1484C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-20C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-318C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-20C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30498
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

1-163044097-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044097
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044097
    reference: chr 1
allele count: 3
allele frequency: 2.474839135456195e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1490C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-312C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-14C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-14C>T
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-163044110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044110
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044110
    reference: chr 1
allele count: 3
allele frequency: 2.473370049137618e-5
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.379-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.325-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.325-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.212-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.518-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-299G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1503G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.670-1G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.325-1G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: c.670-1G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

1-163044119-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044119
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044119
    reference: chr 1
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.333G>C
  hgvsp: ENST00000367906.3:c.333G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.526G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-290G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.678G>C
  hgvsp: ENST00000421743.2:c.678G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.333G>C
  hgvsp: ENST00000527809.1:c.333G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.220G>C
  hgvsp: ENSP00000356884.4:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.333G>C
  hgvsp: ENST00000528938.1:c.333G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1512G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.387G>C
  hgvsp: ENST00000367909.6:c.387G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly74Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

1-163044132-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044132
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044132
    reference: chr 1
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.346A>T
  hgvsp: ENSP00000356882.3:p.Arg116Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.346A>T
  hgvsp: ENSP00000432194.1:p.Arg116Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.233A>T
  hgvsp: ENSP00000356884.4:p.Gln78Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.346A>T
  hgvsp: ENSP00000433261.1:p.Arg116Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-277A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1525A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.400A>T
  hgvsp: ENSP00000356885.6:p.Arg134Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.691A>T
  hgvsp: ENSP00000397181.2:p.Arg231Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000533019
  gene symbol: RGS4
  hgvsc: ENST00000533019.1:n.539A>T
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2716
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg231Trp
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

1-163044136-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044136
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044136
    reference: chr 1
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.350A>T
  hgvsp: ENSP00000432194.1:p.Glu117Val
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1529A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.350A>T
  hgvsp: ENSP00000433261.1:p.Glu117Val
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.350A>T
  hgvsp: ENSP00000356882.3:p.Glu117Val
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.237A>T
  hgvsp: ENST00000367908.4:c.237A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.404A>T
  hgvsp: ENSP00000356885.6:p.Glu135Val
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-273A>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.695A>T
  hgvsp: ENSP00000397181.2:p.Glu232Val
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu232Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-163044138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044138
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044138
    reference: chr 1
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.406G>C
  hgvsp: ENSP00000356885.6:p.Glu136Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.352G>C
  hgvsp: ENSP00000433261.1:p.Glu118Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.697G>C
  hgvsp: ENSP00000397181.2:p.Glu233Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1531G>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.239G>C
  hgvsp: ENSP00000356884.4:p.Arg80Thr
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.352G>C
  hgvsp: ENSP00000356882.3:p.Glu118Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.352G>C
  hgvsp: ENSP00000432194.1:p.Glu118Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-271G>C
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu233Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-163044141-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044141
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044141
    reference: chr 1
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.409A>G
  hgvsp: ENSP00000356885.6:p.Thr137Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-268A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.355A>G
  hgvsp: ENSP00000432194.1:p.Thr119Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.700A>G
  hgvsp: ENSP00000397181.2:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.355A>G
  hgvsp: ENSP00000356882.3:p.Thr119Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.242A>G
  hgvsp: ENSP00000356884.4:p.Asp81Gly
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.355A>G
  hgvsp: ENSP00000433261.1:p.Thr119Ala
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1534A>G
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr234Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-163044147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044147
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044147
    reference: chr 1
allele count: 38
allele frequency: 3.131076760818694e-4
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.361C>T
  hgvsp: ENSP00000432194.1:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1540C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.706C>T
  hgvsp: ENSP00000397181.2:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.248C>T
  hgvsp: ENSP00000356884.4:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.415C>T
  hgvsp: ENSP00000356885.6:p.Arg139Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.361C>T
  hgvsp: ENSP00000356882.3:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-262C>T
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.361C>T
  hgvsp: ENSP00000433261.1:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41691
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg236Trp
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-163044148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044148
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044148
    reference: chr 1
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1541G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.362G>A
  hgvsp: ENSP00000432194.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.249G>A
  hgvsp: ENST00000367908.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-261G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.416G>A
  hgvsp: ENSP00000356885.6:p.Arg139Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.362G>A
  hgvsp: ENSP00000356882.3:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.707G>A
  hgvsp: ENSP00000397181.2:p.Arg236Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.362G>A
  hgvsp: ENSP00000433261.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41714
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg236Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-163044154-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044154
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044154
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-255T>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.368T>A
  hgvsp: ENSP00000433261.1:p.Met123Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.713T>A
  hgvsp: ENSP00000397181.2:p.Met238Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.255T>A
  hgvsp: ENSP00000356884.4:p.His85Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.422T>A
  hgvsp: ENSP00000356885.6:p.Met141Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.368T>A
  hgvsp: ENSP00000356882.3:p.Met123Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.368T>A
  hgvsp: ENSP00000432194.1:p.Met123Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1547T>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41718
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met238Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

1-163044178-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044178
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044178
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.446T>C
  hgvsp: ENSP00000356885.6:p.Phe149Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1571T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.392T>C
  hgvsp: ENSP00000432194.1:p.Phe131Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.279T>C
  hgvsp: ENST00000367908.4:c.279T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.392T>C
  hgvsp: ENSP00000433261.1:p.Phe131Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-231T>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.737T>C
  hgvsp: ENSP00000397181.2:p.Phe246Ser
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.392T>C
  hgvsp: ENSP00000356882.3:p.Phe131Ser
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe246Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

1-163044183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044183
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044183
    reference: chr 1
allele count: 10
allele frequency: 8.237503706876669e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.742G>A
  hgvsp: ENSP00000397181.2:p.Glu248Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.397G>A
  hgvsp: ENSP00000356882.3:p.Glu133Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-226G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.397G>A
  hgvsp: ENSP00000433261.1:p.Glu133Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.451G>A
  hgvsp: ENSP00000356885.6:p.Glu151Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.397G>A
  hgvsp: ENSP00000432194.1:p.Glu133Lys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1576G>A
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.*2G>A
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41733
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu248Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-163044195-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044195
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044195
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.409A>C
  hgvsp: ENSP00000432194.1:p.Lys137Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-214A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.409A>C
  hgvsp: ENSP00000356882.3:p.Lys137Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.463A>C
  hgvsp: ENSP00000356885.6:p.Lys155Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.*14A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.754A>C
  hgvsp: ENSP00000397181.2:p.Lys252Gln
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1588A>C
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.409A>C
  hgvsp: ENSP00000433261.1:p.Lys137Gln
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys252Gln
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

1-163044216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044216
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044216
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1609A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000432194
  ensembl transcript: ENST00000528938
  gene symbol: RGS4
  hgvsc: ENST00000528938.1:c.430A>G
  hgvsp: ENST00000528938.1:c.430A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.430A>G
  hgvsp: ENSP00000433261.1:p.Lys144Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-193A>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.775A>G
  hgvsp: ENSP00000397181.2:p.Lys259Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.484A>G
  hgvsp: ENSP00000356885.6:p.Lys162Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356882
  ensembl transcript: ENST00000367906
  gene symbol: RGS4
  hgvsc: ENST00000367906.3:c.430A>G
  hgvsp: ENSP00000356882.3:p.Lys144Glu
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.*35A>G
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys259Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

1-163044223-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163044223
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 163044223
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000433261
  ensembl transcript: ENST00000527809
  gene symbol: RGS4
  hgvsc: ENST00000527809.1:c.437C>G
  hgvsp: ENSP00000433261.1:p.Ser146Cys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356884
  ensembl transcript: ENST00000367908
  gene symbol: RGS4
  hgvsc: ENST00000367908.4:c.*42C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000436106
  ensembl transcript: ENST00000531057
  gene symbol: RGS4
  hgvsc: ENST00000531057.1:c.331-186C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000117152
  ensembl transcript: ENST00000491263
  gene symbol: RGS4
  hgvsc: ENST00000491263.1:n.1616C>G
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000397181
  ensembl transcript: ENST00000421743
  gene symbol: RGS4
  hgvsc: ENST00000421743.2:c.782C>G
  hgvsp: ENSP00000397181.2:p.Ser261Cys
  variant of: http://identifiers.org/hgnc/10000
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117152
  ensembl protein: ENSP00000356885
  ensembl transcript: ENST00000367909
  gene symbol: RGS4
  hgvsc: ENST00000367909.6:c.491C>G
  hgvsp: ENSP00000356885.6:p.Ser164Cys
  variant of: http://identifiers.org/hgnc/10000
canonical: true
consequence: missense
filter: PASS
hgvs: p.Ser261Cys
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179801793298726e-4
allele num: 8476
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.57e-1

DP
type: SiteQuality
SIO_000300: 1.624022e6

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.808e1

VQSLOD
type: SiteQuality
SIO_000300: -1.764e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 8.515000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.78e-1

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 720
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42705
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510756586898719e-5
allele num: 66192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.820000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.058e0

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

FS
type: SiteQuality
SIO_000300: 1.643e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

DP
type: SiteQuality
SIO_000300: 1.622094e6

GenotypeDepth
all individuals: 504
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4607
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66192
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

FS
type: SiteQuality
SIO_000300: 3.336e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.621443e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 749
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511578692786746e-5
allele num: 66156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.474e0

QD
type: SiteQuality
SIO_000300: 1.126e1

DP
type: SiteQuality
SIO_000300: 1.620135e6

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.26e-1

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5596
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 181
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1654
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516484183069971e-5
allele num: 65942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.189e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 7.44e0

FS
type: SiteQuality
SIO_000300: 7.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.786e0

DP
type: SiteQuality
SIO_000300: 1.606454e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

GenotypeQuality
all individuals: 1634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.153846153846154e-5
allele num: 16250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

DP
type: SiteQuality
SIO_000300: 1.592531e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 8.34e0

FS
type: SiteQuality
SIO_000300: 2.877e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 520
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519618271890101e-5
allele num: 65806
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 8.34e0

FS
type: SiteQuality
SIO_000300: 2.877e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

DP
type: SiteQuality
SIO_000300: 1.592531e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2273
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.461841457410143e-4
allele num: 16248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520958812435359e-5
allele num: 65748
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 4.212e0

DP
type: SiteQuality
SIO_000300: 1.571055e6

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.189e1

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

GenotypeQuality
all individuals: 759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5119
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 32914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191327138432213e-4
allele num: 8394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.847e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

QD
type: SiteQuality
SIO_000300: 1.076e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.219e0

VQSLOD
type: SiteQuality
SIO_000300: -2.384e0

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

DP
type: SiteQuality
SIO_000300: 1.547786e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

GenotypeQuality
all individuals: 940
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2769
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523461304082876e-5
allele num: 65640
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.177e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.317e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

VQSLOD
type: SiteQuality
SIO_000300: -7.62e-2

DP
type: SiteQuality
SIO_000300: 1.542565e6

FS
type: SiteQuality
SIO_000300: 7.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 1033
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2880
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528631263566603e-5
allele num: 65418
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.45e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 3.565e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 1.508049e6

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

GenotypeQuality
all individuals: 4599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 448
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4991
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.200480192076831e-4
allele num: 8330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65224
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16050
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.576e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -2.501e-1

DP
type: SiteQuality
SIO_000300: 1.49475e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.445e0

MQRankSum
type: SiteQuality
SIO_000300: -1.818e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 1.235e1

GenotypeQuality
all individuals: 246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4098
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19194
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2950
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.235969069593415e-5
allele num: 16036
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.675e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.549e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.31e1

DP
type: SiteQuality
SIO_000300: 1.493753e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.622e0

GenotypeQuality
all individuals: 3429
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40726
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64106
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.81057268722467e-5
allele num: 11350
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.067e0

VQSLOD
type: SiteQuality
SIO_000300: 4.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 1.695587e6

GenotypeQuality
all individuals: 794
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3428
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40746
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1812
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55938123752495e-5
allele num: 64128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.12e1

VQSLOD
type: SiteQuality
SIO_000300: -1.494e0

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

FS
type: SiteQuality
SIO_000300: 1.165e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.309e0

DP
type: SiteQuality
SIO_000300: 1.695819e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 6897
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 662
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40779
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.073883161512027e-4
allele num: 9312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64134
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 1.696356e6

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 1.037e1

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

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3420
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6895
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.1629e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.109e1

DP
type: SiteQuality
SIO_000300: 1.700561e6

VQSLOD
type: SiteQuality
SIO_000300: -4.618e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

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

GenotypeQuality
all individuals: 210
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6895
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40852
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557972143458075e-5
allele num: 64186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.700561e6

QD
type: SiteQuality
SIO_000300: 1.109e1

VQSLOD
type: SiteQuality
SIO_000300: -4.618e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.1629e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

GenotypeQuality
all individuals: 2482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40864
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64188
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.805917576611483e-5
allele num: 11356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.701141e6

QD
type: SiteQuality
SIO_000300: 1.241e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 4.023e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.493e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.303e0

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

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3415
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3007
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40908
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.063809748057452e-4
allele num: 8494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.436e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

DP
type: SiteQuality
SIO_000300: 1.704396e6

GenotypeQuality
all individuals: 692
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3326
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1383
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
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: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64298
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 7.235e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.455e0

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

DP
type: SiteQuality
SIO_000300: 1.706486e6

QD
type: SiteQuality
SIO_000300: 5.69e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

GenotypeQuality
all individuals: 226
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3394
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6894
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.669302407309787e-3
allele num: 11382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.368e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

FS
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

DP
type: SiteQuality
SIO_000300: 1.707702e6

GenotypeQuality
all individuals: 3388
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 254
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40974
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554388037429664e-5
allele num: 64334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.312e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.622e0

DP
type: SiteQuality
SIO_000300: 1.706518e6

QD
type: SiteQuality
SIO_000300: 1.168e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 255
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.657951122566221e-5
allele num: 64406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.64e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.135e0

MQRankSum
type: SiteQuality
SIO_000300: 9.44e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 1.709003e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551879325863621e-5
allele num: 64438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.678e0

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.709606e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.199e0

VQSLOD
type: SiteQuality
SIO_000300: -6.525e-1

FS
type: SiteQuality
SIO_000300: 9.31e0

QD
type: SiteQuality
SIO_000300: 1.158e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

GenotypeQuality
all individuals: 3382
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6904
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175088131609871e-4
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.103084465959163e-5
allele num: 64452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 5.182e0

DP
type: SiteQuality
SIO_000300: 1.70985e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.147e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeQuality
all individuals: 322
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6901
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1319
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547891771407343e-5
allele num: 64604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
SIO_000300: 9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.714277e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 41161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3378
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10782
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545356204605162e-5
allele num: 64710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.276e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 3.688e0

VQSLOD
type: SiteQuality
SIO_000300: 7.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 1.716205e6

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6919
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3377
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65206
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.758101243650377e-5
allele num: 11418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12134
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.412e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

FS
type: SiteQuality
SIO_000300: 1.355e0

DP
type: SiteQuality
SIO_000300: 1.731649e6

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6922
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3377
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12588
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.625590757920532e-4
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.406e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.843e0

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
SIO_000300: 1.737498e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 7.14e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

GenotypeQuality
all individuals: 1387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44742
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7008
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511578692786746e-5
allele num: 66156
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.768041e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

FS
type: SiteQuality
SIO_000300: 5.238e0

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 44989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7022
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.496881496881497e-5
allele num: 15392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.589e0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 1.855e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

DP
type: SiteQuality
SIO_000300: 1.772133e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.196e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017137340091721e-5
allele num: 66288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.682e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.245e1

DP
type: SiteQuality
SIO_000300: 1.774006e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 798
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15640
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.799e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.605e0

QD
type: SiteQuality
SIO_000300: 1.394e1

FS
type: SiteQuality
SIO_000300: 1.1139e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

DP
type: SiteQuality
SIO_000300: 1.774716e6

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.506614035616356e-4
allele num: 66374
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.359e1

DP
type: SiteQuality
SIO_000300: 1.778437e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.236e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 2.786e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 1332
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.777825e6

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.307e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.205e-1

QD
type: SiteQuality
SIO_000300: 7.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.59e-1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45490
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7036
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 1.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

QD
type: SiteQuality
SIO_000300: 1.551e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.58e-1

DP
type: SiteQuality
SIO_000300: 1.777796e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -6.064000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

QD
type: SiteQuality
SIO_000300: 1.512e1

FS
type: SiteQuality
SIO_000300: 1.456e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.898e0

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 1.775414e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511990081345066e-5
allele num: 66138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.024e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

QD
type: SiteQuality
SIO_000300: 6.8e0

DP
type: SiteQuality
SIO_000300: 1.768985e6

VQSLOD
type: SiteQuality
SIO_000300: -1.052e0

GenotypeQuality
all individuals: 1696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6772
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65708
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.751105e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.246e0

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

FS
type: SiteQuality
SIO_000300: 7.009e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.287e-1

QD
type: SiteQuality
SIO_000300: 9.720000000000001e0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65368
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.941747572815534e-4
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.538e1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 1.734476e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 6220
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575994452499527e-5
allele num: 63452
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.911e0

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.661684e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.704390509953641e-5
allele num: 58672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11870
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

QD
type: SiteQuality
SIO_000300: 3.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.485776e6

VQSLOD
type: SiteQuality
SIO_000300: -2.275e0

FS
type: SiteQuality
SIO_000300: 2.887e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

GenotypeQuality
all individuals: 444
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9668
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.150218541522889e-4
allele num: 8694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53386
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

DP
type: SiteQuality
SIO_000300: 1.268211e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.2545e1

QD
type: SiteQuality
SIO_000300: 1.341e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e0

VQSLOD
type: SiteQuality
SIO_000300: -5.886e-1

GenotypeQuality
all individuals: 530
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24908
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2040
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.341e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

DP
type: SiteQuality
SIO_000300: 1.228206e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.669e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.816e0

GenotypeQuality
all individuals: 257
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29048
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4989
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 7.742934572202865e-4
allele num: 5166
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

DP
type: SiteQuality
SIO_000300: 9.90597e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

QD
type: SiteQuality
SIO_000300: 1.803e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4977
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7720
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25691
bin: 2.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.684798305574275e-4
allele num: 41548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

DP
type: SiteQuality
SIO_000300: 9.00839e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.112e0

QD
type: SiteQuality
SIO_000300: 1.124e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4597
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8060
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3748
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7420
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.887585532746823e-5
allele num: 40920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.031e0

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

DP
type: SiteQuality
SIO_000300: 8.90564e5

FS
type: SiteQuality
SIO_000300: 4.781e0

QD
type: SiteQuality
SIO_000300: 1.152e1

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

GenotypeQuality
all individuals: 788
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22011
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2905
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.216756220981794e-5
allele num: 38338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.69e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.175e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 8.53217e5

QD
type: SiteQuality
SIO_000300: 7.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

GenotypeQuality
all individuals: 7853
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5499
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14543
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33090
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.798561151079137e-4
allele num: 5560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

DP
type: SiteQuality
SIO_000300: 8.19712e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 7.34e0

GenotypeQuality
all individuals: 40987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 268
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8972
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

DP
type: SiteQuality
SIO_000300: 1.743374e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9049
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.749979e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.185e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

QD
type: SiteQuality
SIO_000300: 3.094e1

GenotypeQuality
all individuals: 1389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41528
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

QD
type: SiteQuality
SIO_000300: 3.16e0

VQSLOD
type: SiteQuality
SIO_000300: -3.249e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.753009e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41609
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
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: 8628
num of homozygotes: 0

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
allele num: 11496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

FS
type: SiteQuality
SIO_000300: 1.204e0

DP
type: SiteQuality
SIO_000300: 1.75428e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeQuality
all individuals: 2298
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9125
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41585
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
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: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.755126e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.263e0

FS
type: SiteQuality
SIO_000300: 2.974e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2159
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41616
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

FS
type: SiteQuality
SIO_000300: 6.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

DP
type: SiteQuality
SIO_000300: 1.757053e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.002000000000001e0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2171
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2328
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9181
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497616263380409e-5
allele num: 66702
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.427e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

FS
type: SiteQuality
SIO_000300: 1.375e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

DP
type: SiteQuality
SIO_000300: 1.758733e6

QD
type: SiteQuality
SIO_000300: 1.552e1

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2169
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 605
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.759007e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.151e0

QD
type: SiteQuality
SIO_000300: 1.286e1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.609e0

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

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2170
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 41667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 1.75952e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

FS
type: SiteQuality
SIO_000300: 2.249e0

QD
type: SiteQuality
SIO_000300: 1.653e1

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

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

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

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41667
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

MQ
type: SiteQuality
SIO_000300: 5.991e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

FS
type: SiteQuality
SIO_000300: 1.1098e1

VQSLOD
type: SiteQuality
SIO_000300: -1.638e0

QD
type: SiteQuality
SIO_000300: 1.212e1

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.759462e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 2719
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 9188
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 8.266999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 1.759295e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.108e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.474e0

QD
type: SiteQuality
SIO_000300: 1.567e1

GenotypeQuality
all individuals: 2717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

FS
type: SiteQuality
SIO_000300: 5.769e0

DP
type: SiteQuality
SIO_000300: 1.759395e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

VQSLOD
type: SiteQuality
SIO_000300: -1.888e0

QD
type: SiteQuality
SIO_000300: 1.494e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.048e0

GenotypeQuality
all individuals: 602
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 1439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2168
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9187
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 30
allele frequency: 3.469812630117973e-3
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.44e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.76459e6

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2719
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1440
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9193
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2342
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.925e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.674e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.715e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 4.88e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

DP
type: SiteQuality
SIO_000300: 1.756415e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 9194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1439
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.427e1

MQRankSum
type: SiteQuality
SIO_000300: -6.850000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 1.756486e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

FS
type: SiteQuality
SIO_000300: 1.543e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.107e0

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41733
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.53e0

DP
type: SiteQuality
SIO_000300: 1.756532e6

VQSLOD
type: SiteQuality
SIO_000300: -8.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.405e0

MQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.315e1

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

GenotypeQuality
all individuals: 9195
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2134
bin: 9.75e1
variant carriers: 10

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498531439189594e-4
allele num: 66732
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

QD
type: SiteQuality
SIO_000300: 1.299e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.758171e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.127e0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9195
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 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: 11570
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.756113e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.569e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

VQSLOD
type: SiteQuality
SIO_000300: -3.448e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.239e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e0

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2718
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9197
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41738
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 1.755955e6

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.94e0

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.268e0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1