1-240975275-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975275
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975275
    reference: chr 1
allele count: 7
allele frequency: 5.768153202149049e-5
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.1025T>C
  hgvsp: ENSP00000355520.4:p.Val342Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.866T>C
  hgvsp: ENSP00000385508.1:p.Val289Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.1025T>C
  hgvsp: ENSP00000355522.1:p.Val342Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.1025T>C
  hgvsp: ENSP00000355521.1:p.Val342Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.1025T>C
  hgvsp: ENSP00000355523.1:p.Val342Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.518T>C
  hgvsp: ENSP00000404399.1:p.Val173Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.773T>C
  hgvsp: ENSP00000390138.2:p.Val258Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.1025T>C
  hgvsp: ENSP00000384428.1:p.Val342Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.866T>C
  hgvsp: ENSP00000341242.2:p.Val289Ala
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.947T>C
  hgvsp: ENSP00000331485.7:p.Val316Ala
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val342Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-240975275-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975275
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975275
    reference: chr 1
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.1025T>G
  hgvsp: ENSP00000355520.4:p.Val342Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.866T>G
  hgvsp: ENSP00000385508.1:p.Val289Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.1025T>G
  hgvsp: ENSP00000384428.1:p.Val342Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.1025T>G
  hgvsp: ENSP00000355521.1:p.Val342Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.1025T>G
  hgvsp: ENSP00000355522.1:p.Val342Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.866T>G
  hgvsp: ENSP00000341242.2:p.Val289Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.773T>G
  hgvsp: ENSP00000390138.2:p.Val258Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.947T>G
  hgvsp: ENSP00000331485.7:p.Val316Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.518T>G
  hgvsp: ENSP00000404399.1:p.Val173Gly
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.1025T>G
  hgvsp: ENSP00000355523.1:p.Val342Gly
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val342Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/1-240975276-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975276
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975276
    reference: chr 1
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.865G>T
  hgvsp: ENSP00000341242.2:p.Val289Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.1024G>T
  hgvsp: ENSP00000355523.1:p.Val342Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.1024G>T
  hgvsp: ENSP00000355522.1:p.Val342Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.1024G>T
  hgvsp: ENSP00000355521.1:p.Val342Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.1024G>T
  hgvsp: ENSP00000384428.1:p.Val342Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.517G>T
  hgvsp: ENSP00000404399.1:p.Val173Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.946G>T
  hgvsp: ENSP00000331485.7:p.Val316Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.865G>T
  hgvsp: ENSP00000385508.1:p.Val289Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.772G>T
  hgvsp: ENSP00000390138.2:p.Val258Phe
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.1024G>T
  hgvsp: ENSP00000355520.4:p.Val342Phe
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val342Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-240975292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975292
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975292
    reference: chr 1
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.849G>A
  hgvsp: ENST00000348120.2:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.930G>A
  hgvsp: ENST00000331110.7:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.1008G>A
  hgvsp: ENST00000407727.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.1008G>A
  hgvsp: ENST00000366565.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.756G>A
  hgvsp: ENST00000446183.2:c.756G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.849G>A
  hgvsp: ENST00000401882.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.1008G>A
  hgvsp: ENST00000366564.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.1008G>A
  hgvsp: ENST00000366562.4:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.1008G>A
  hgvsp: ENST00000366563.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.501G>A
  hgvsp: ENST00000440928.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu336Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

1-240975295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975295
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975295
    reference: chr 1
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.753C>T
  hgvsp: ENST00000446183.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.846C>T
  hgvsp: ENST00000401882.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.1005C>T
  hgvsp: ENST00000366564.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.927C>T
  hgvsp: ENST00000331110.7:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.1005C>T
  hgvsp: ENST00000366565.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.1005C>T
  hgvsp: ENST00000366562.4:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.846C>T
  hgvsp: ENST00000348120.2:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.498C>T
  hgvsp: ENST00000440928.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.1005C>T
  hgvsp: ENST00000366563.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.1005C>T
  hgvsp: ENST00000407727.1:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp335Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-240975314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975314
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975314
    reference: chr 1
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.986G>A
  hgvsp: ENSP00000384428.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.986G>A
  hgvsp: ENSP00000355522.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.908G>A
  hgvsp: ENSP00000331485.7:p.Arg303Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.986G>A
  hgvsp: ENSP00000355520.4:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.479G>A
  hgvsp: ENSP00000404399.1:p.Arg160Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.827G>A
  hgvsp: ENSP00000341242.2:p.Arg276Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.827G>A
  hgvsp: ENSP00000385508.1:p.Arg276Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.734G>A
  hgvsp: ENSP00000390138.2:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.986G>A
  hgvsp: ENSP00000355521.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.986G>A
  hgvsp: ENSP00000355523.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg329Gln
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

1-240975323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975323
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975323
    reference: chr 1
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.977G>A
  hgvsp: ENSP00000355521.1:p.Arg326Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.899G>A
  hgvsp: ENSP00000331485.7:p.Arg300Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.977G>A
  hgvsp: ENSP00000355520.4:p.Arg326Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.818G>A
  hgvsp: ENSP00000341242.2:p.Arg273Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.818G>A
  hgvsp: ENSP00000385508.1:p.Arg273Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.725G>A
  hgvsp: ENSP00000390138.2:p.Arg242Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.977G>A
  hgvsp: ENSP00000384428.1:p.Arg326Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.977G>A
  hgvsp: ENSP00000355523.1:p.Arg326Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.977G>A
  hgvsp: ENSP00000355522.1:p.Arg326Lys
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.470G>A
  hgvsp: ENSP00000404399.1:p.Arg157Lys
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg326Lys
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: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-240975334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975334
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975334
    reference: chr 1
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.807G>A
  hgvsp: ENST00000401882.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.966G>A
  hgvsp: ENST00000366563.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.888G>A
  hgvsp: ENST00000331110.7:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.807G>A
  hgvsp: ENST00000348120.2:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.966G>A
  hgvsp: ENST00000407727.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.966G>A
  hgvsp: ENST00000366565.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.714G>A
  hgvsp: ENST00000446183.2:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.459G>A
  hgvsp: ENST00000440928.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.966G>A
  hgvsp: ENST00000366562.4:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.966G>A
  hgvsp: ENST00000366564.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro322Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-240975335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975335
    reference: chr 1
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.713C>T
  hgvsp: ENSP00000390138.2:p.Pro238Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.806C>T
  hgvsp: ENSP00000385508.1:p.Pro269Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.806C>T
  hgvsp: ENSP00000341242.2:p.Pro269Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.965C>T
  hgvsp: ENSP00000355521.1:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.887C>T
  hgvsp: ENSP00000331485.7:p.Pro296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.965C>T
  hgvsp: ENSP00000384428.1:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.965C>T
  hgvsp: ENSP00000355522.1:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.965C>T
  hgvsp: ENSP00000355523.1:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.458C>T
  hgvsp: ENSP00000404399.1:p.Pro153Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.965C>T
  hgvsp: ENSP00000355520.4:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro322Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-240975346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975346
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975346
    reference: chr 1
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-3T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-3T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2819
  bin: 8.25e1
  variant carriers: 0
hgvs: c.957-3T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

1-240975356-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975356
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975356
    reference: chr 1
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-13T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-13T>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 7.25e1
  variant carriers: 0
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: A
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-240975358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975358
    reference: chr 1
allele count: 93
allele frequency: 7.667700019787613e-4
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-15T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-15T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 5236
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43283
  bin: 9.75e1
  variant carriers: 93
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS

1-240975364-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975364
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975364
    reference: chr 1
allele count: 4
allele frequency: 3.298479400996141e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-21C>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-21C>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-240975367-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975367
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975367
    reference: chr 1
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-24T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6664
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-240975368-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975368
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975368
    reference: chr 1
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-25T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-25T>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

1-240975381-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975381
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975381
    reference: chr 1
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-38T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-38T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-240975381-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975381
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975381
    reference: chr 1
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-38T>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-38T>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-240975385-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975385
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975385
    reference: chr 1
allele count: 15
allele frequency: 1.237950614023505e-4
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-42C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-42C>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43240
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-240975385-G-GGCAAGTTTTAAAAATATATAAAGATGATGTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975385
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975417
    reference: chr 1
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: GGCAAGTTTTAAAAATATATAAAGATGATGTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43240
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-240975393-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240975393
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240975394
    reference: chr 1
allele count: 2
allele frequency: 1.65169133192389e-5
allele num: 121088
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.957-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.957-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.705-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.798-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.798-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.957-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.450-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.957-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.879-51dupA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.957-51dupA
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

1-240976873-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976873
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976873
    reference: chr 1
allele count: 1
allele frequency: 9.411587546587358e-6
allele num: 106252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+45A>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6741
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6801
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-240976878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976878
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976878
    reference: chr 1
allele count: 49
allele frequency: 4.581665856303998e-4
allele num: 106948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+40A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+40A>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15604
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15094
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

1-240976888-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976888
    reference: chr 1
allele count: 2
allele frequency: 1.842672612356962e-5
allele num: 108538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+30A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+30A>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24372
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

1-240976894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976894
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976894
    reference: chr 1
allele count: 2
allele frequency: 1.81801654395055e-5
allele num: 110010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+24G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+24G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-240976895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976895
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976895
    reference: chr 1
allele count: 13
allele frequency: 1.173306377371433e-4
allele num: 110798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+23C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+23C>T
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29464
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-240976910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976910
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976910
    reference: chr 1
allele count: 1
allele frequency: 8.552271483305966e-6
allele num: 116928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.956+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.797+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.956+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.797+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.704+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.449+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.956+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.956+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.878+8G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.956+8G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9093
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
hgvs: c.956+8G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
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: ClippingRankSum
site quality: QD
site quality: MQ

1-240976921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976921
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976921
    reference: chr 1
allele count: 8
allele frequency: 6.664334149714266e-5
allele num: 120042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.953C>T
  hgvsp: ENSP00000355521.1:p.Ala318Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.953C>T
  hgvsp: ENSP00000355520.4:p.Ala318Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.701C>T
  hgvsp: ENSP00000390138.2:p.Ala234Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.794C>T
  hgvsp: ENSP00000385508.1:p.Ala265Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.875C>T
  hgvsp: ENSP00000331485.7:p.Ala292Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.953C>T
  hgvsp: ENSP00000384428.1:p.Ala318Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.953C>T
  hgvsp: ENSP00000355522.1:p.Ala318Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.794C>T
  hgvsp: ENSP00000341242.2:p.Ala265Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.953C>T
  hgvsp: ENSP00000355523.1:p.Ala318Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.446C>T
  hgvsp: ENSP00000404399.1:p.Ala149Val
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10291
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46028
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala318Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

1-240976923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976923
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976923
    reference: chr 1
allele count: 13
allele frequency: 1.081224944691186e-4
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.951G>A
  hgvsp: ENST00000366564.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.444G>A
  hgvsp: ENST00000440928.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.951G>A
  hgvsp: ENST00000366565.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.951G>A
  hgvsp: ENST00000366563.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.873G>A
  hgvsp: ENST00000331110.7:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.792G>A
  hgvsp: ENST00000401882.1:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.792G>A
  hgvsp: ENST00000348120.2:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.699G>A
  hgvsp: ENST00000446183.2:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.951G>A
  hgvsp: ENST00000407727.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.951G>A
  hgvsp: ENST00000366562.4:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu317Glu
num of homozygotes: 1
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

1-240976950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976950
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976950
    reference: chr 1
allele count: 4
allele frequency: 3.301964668978042e-5
allele num: 121140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.924C>T
  hgvsp: ENST00000366564.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.846C>T
  hgvsp: ENST00000331110.7:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.924C>T
  hgvsp: ENST00000366565.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.924C>T
  hgvsp: ENST00000366563.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.765C>T
  hgvsp: ENST00000348120.2:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.765C>T
  hgvsp: ENST00000401882.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.924C>T
  hgvsp: ENST00000366562.4:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.672C>T
  hgvsp: ENST00000446183.2:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.417C>T
  hgvsp: ENST00000440928.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.924C>T
  hgvsp: ENST00000407727.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser308Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

1-240976953-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976953
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976953
    reference: chr 1
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.762G>A
  hgvsp: ENST00000348120.2:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.921G>A
  hgvsp: ENST00000366563.1:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.762G>A
  hgvsp: ENST00000401882.1:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.669G>A
  hgvsp: ENST00000446183.2:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.921G>A
  hgvsp: ENST00000366565.1:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.843G>A
  hgvsp: ENST00000331110.7:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.414G>A
  hgvsp: ENST00000440928.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.921G>A
  hgvsp: ENST00000366562.4:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.921G>A
  hgvsp: ENST00000366564.1:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.921G>A
  hgvsp: ENST00000407727.1:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu307Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-240976961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976961
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976961
    reference: chr 1
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.913C>T
  hgvsp: ENSP00000355522.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.661C>T
  hgvsp: ENSP00000390138.2:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.406C>T
  hgvsp: ENSP00000404399.1:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.754C>T
  hgvsp: ENSP00000385508.1:p.Pro252Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.913C>T
  hgvsp: ENSP00000384428.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.913C>T
  hgvsp: ENSP00000355523.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.754C>T
  hgvsp: ENSP00000341242.2:p.Pro252Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.835C>T
  hgvsp: ENSP00000331485.7:p.Pro279Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.913C>T
  hgvsp: ENSP00000355521.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.913C>T
  hgvsp: ENSP00000355520.4:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro305Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

1-240976976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976976
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976976
    reference: chr 1
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.898C>T
  hgvsp: ENSP00000355523.1:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.898C>T
  hgvsp: ENSP00000384428.1:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.391C>T
  hgvsp: ENSP00000404399.1:p.Pro131Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.739C>T
  hgvsp: ENSP00000341242.2:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.739C>T
  hgvsp: ENSP00000385508.1:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.898C>T
  hgvsp: ENSP00000355522.1:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.646C>T
  hgvsp: ENSP00000390138.2:p.Pro216Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.898C>T
  hgvsp: ENSP00000355521.1:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.898C>T
  hgvsp: ENSP00000355520.4:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.820C>T
  hgvsp: ENSP00000331485.7:p.Pro274Ser
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro300Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-240976986-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976986
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976986
    reference: chr 1
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.888T>A
  hgvsp: ENSP00000355521.1:p.Phe296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.888T>A
  hgvsp: ENSP00000355523.1:p.Phe296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.888T>A
  hgvsp: ENSP00000355522.1:p.Phe296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.381T>A
  hgvsp: ENSP00000404399.1:p.Phe127Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.888T>A
  hgvsp: ENSP00000384428.1:p.Phe296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.729T>A
  hgvsp: ENSP00000341242.2:p.Phe243Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.888T>A
  hgvsp: ENSP00000355520.4:p.Phe296Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.810T>A
  hgvsp: ENSP00000331485.7:p.Phe270Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.729T>A
  hgvsp: ENSP00000385508.1:p.Phe243Leu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.636T>A
  hgvsp: ENSP00000390138.2:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37944
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe296Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-240976989-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976989
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976989
    reference: chr 1
allele count: 2
allele frequency: 1.65174589541145e-5
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.885G>A
  hgvsp: ENST00000366562.4:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.633G>A
  hgvsp: ENST00000446183.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.885G>A
  hgvsp: ENST00000366563.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.726G>A
  hgvsp: ENST00000348120.2:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.885G>A
  hgvsp: ENST00000407727.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.885G>A
  hgvsp: ENST00000366564.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.378G>A
  hgvsp: ENST00000440928.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.807G>A
  hgvsp: ENST00000331110.7:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.726G>A
  hgvsp: ENST00000401882.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.885G>A
  hgvsp: ENST00000366565.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro295Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-240976994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240976994
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240976994
    reference: chr 1
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.880G>A
  hgvsp: ENSP00000355522.1:p.Asp294Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.721G>A
  hgvsp: ENSP00000341242.2:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.721G>A
  hgvsp: ENSP00000385508.1:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.880G>A
  hgvsp: ENSP00000355521.1:p.Asp294Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.373G>A
  hgvsp: ENSP00000404399.1:p.Asp125Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.628G>A
  hgvsp: ENSP00000390138.2:p.Asp210Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.880G>A
  hgvsp: ENSP00000355523.1:p.Asp294Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.802G>A
  hgvsp: ENSP00000331485.7:p.Asp268Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.880G>A
  hgvsp: ENSP00000384428.1:p.Asp294Asn
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.880G>A
  hgvsp: ENSP00000355520.4:p.Asp294Asn
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp294Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-240977003-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977003
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977003
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.871T>G
  hgvsp: ENSP00000355523.1:p.Leu291Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.712T>G
  hgvsp: ENSP00000341242.2:p.Leu238Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.871T>G
  hgvsp: ENSP00000355520.4:p.Leu291Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.871T>G
  hgvsp: ENSP00000355521.1:p.Leu291Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.871T>G
  hgvsp: ENSP00000384428.1:p.Leu291Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.619T>G
  hgvsp: ENSP00000390138.2:p.Leu207Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.712T>G
  hgvsp: ENSP00000385508.1:p.Leu238Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.871T>G
  hgvsp: ENSP00000355522.1:p.Leu291Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.364T>G
  hgvsp: ENSP00000404399.1:p.Leu122Val
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.793T>G
  hgvsp: ENSP00000331485.7:p.Leu265Val
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu291Val
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: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

1-240977007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977007
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977007
    reference: chr 1
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.708G>A
  hgvsp: ENST00000348120.2:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.867G>A
  hgvsp: ENST00000407727.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.867G>A
  hgvsp: ENST00000366563.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.867G>A
  hgvsp: ENST00000366565.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.867G>A
  hgvsp: ENST00000366564.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.789G>A
  hgvsp: ENST00000331110.7:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.867G>A
  hgvsp: ENST00000366562.4:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.615G>A
  hgvsp: ENST00000446183.2:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.708G>A
  hgvsp: ENST00000401882.1:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.360G>A
  hgvsp: ENST00000440928.1:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln289Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-240977013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977013
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977013
    reference: chr 1
allele count: 3
allele frequency: 2.498625755834291e-5
allele num: 120066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.702G>A
  hgvsp: ENST00000401882.1:c.702G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.702G>A
  hgvsp: ENST00000348120.2:c.702G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.861G>A
  hgvsp: ENST00000407727.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.861G>A
  hgvsp: ENST00000366562.4:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.861G>A
  hgvsp: ENST00000366565.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.609G>A
  hgvsp: ENST00000446183.2:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.783G>A
  hgvsp: ENST00000331110.7:c.783G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.861G>A
  hgvsp: ENST00000366564.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.861G>A
  hgvsp: ENST00000366563.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.354G>A
  hgvsp: ENST00000440928.1:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11327
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr287Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

1-240977014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977014
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977014
    reference: chr 1
allele count: 1
allele frequency: 8.354079296920687e-6
allele num: 119702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.860C>T
  hgvsp: ENSP00000355521.1:p.Thr287Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.860C>T
  hgvsp: ENSP00000384428.1:p.Thr287Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.608C>T
  hgvsp: ENSP00000390138.2:p.Thr203Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.353C>T
  hgvsp: ENSP00000404399.1:p.Thr118Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.782C>T
  hgvsp: ENSP00000331485.7:p.Thr261Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.701C>T
  hgvsp: ENSP00000341242.2:p.Thr234Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.701C>T
  hgvsp: ENSP00000385508.1:p.Thr234Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.860C>T
  hgvsp: ENSP00000355523.1:p.Thr287Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.860C>T
  hgvsp: ENSP00000355520.4:p.Thr287Met
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.860C>T
  hgvsp: ENSP00000355522.1:p.Thr287Met
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr287Met
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-240977020-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977020
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977020
    reference: chr 1
allele count: 1
allele frequency: 8.421761832575375e-6
allele num: 118740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.602G>T
  hgvsp: ENSP00000390138.2:p.Ser201Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.695G>T
  hgvsp: ENSP00000385508.1:p.Ser232Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.854G>T
  hgvsp: ENSP00000355523.1:p.Ser285Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.854G>T
  hgvsp: ENSP00000355521.1:p.Ser285Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.776G>T
  hgvsp: ENSP00000331485.7:p.Ser259Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.854G>T
  hgvsp: ENSP00000384428.1:p.Ser285Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.854G>T
  hgvsp: ENSP00000355522.1:p.Ser285Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.695G>T
  hgvsp: ENSP00000341242.2:p.Ser232Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.347G>T
  hgvsp: ENSP00000404399.1:p.Ser116Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.854G>T
  hgvsp: ENSP00000355520.4:p.Ser285Ile
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser285Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-240977024-GTAGACTAAGGAGAAAAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977024
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977007
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 117350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
hgvs: c.846-13_849delTTTTTCTCCTTAGTCTA
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: GTAGACTAAGGAGAAAAA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

1-240977025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977025
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977025
    reference: chr 1
allele count: 1
allele frequency: 8.522243054371911e-6
allele num: 117340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.690A>G
  hgvsp: ENST00000401882.1:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.849A>G
  hgvsp: ENST00000407727.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.690A>G
  hgvsp: ENST00000348120.2:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.342A>G
  hgvsp: ENST00000440928.1:c.342A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.849A>G
  hgvsp: ENST00000366564.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.849A>G
  hgvsp: ENST00000366562.4:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.849A>G
  hgvsp: ENST00000366563.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.849A>G
  hgvsp: ENST00000366565.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.597A>G
  hgvsp: ENST00000446183.2:c.597A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.771A>G
  hgvsp: ENST00000331110.7:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu283Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

1-240977034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977034
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977034
    reference: chr 1
allele count: 1
allele frequency: 8.818964300832511e-6
allele num: 113392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.687-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.339-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.846-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.768-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.594-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.846-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.846-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.846-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.687-6C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.846-6C>T
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9791
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: c.846-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

1-240977036-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977036
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977037
    reference: chr 1
allele count: 1
allele frequency: 8.887308922858158e-6
allele num: 112520
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.768-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.594-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.846-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.339-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.846-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.846-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.846-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.687-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.846-9dupT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.687-9dupT
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33212
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-240977043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977043
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977043
    reference: chr 1
allele count: 2
allele frequency: 1.842638658559057e-5
allele num: 108540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.594-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.687-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.846-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.846-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.687-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.846-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.846-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.339-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.768-15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.846-15G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13267
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1522
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-240977068-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977068
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977068
    reference: chr 1
allele count: 1
allele frequency: 1.045696957021855e-5
allele num: 95630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.846-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.339-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.687-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.846-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.687-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.846-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.594-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.846-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.768-40T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.846-40T>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

1-240977078-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977078
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977078
    reference: chr 1
allele count: 2
allele frequency: 2.195196909162752e-5
allele num: 91108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.687-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.339-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.846-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.768-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.594-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.846-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.687-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.846-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.846-50G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.846-50G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11798
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5737
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6290
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-240977970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977970
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977970
    reference: chr 1
allele count: 1
allele frequency: 8.42715566641947e-6
allele num: 118664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+46C>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+46C>T
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

1-240977971-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977971
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977971
    reference: chr 1
allele count: 18
allele frequency: 1.515815003200054e-4
allele num: 118748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+45A>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+45A>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12143
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

1-240977972-C-CATATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977972
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977977
    reference: chr 1
allele count: 13
allele frequency: 1.094976584346889e-4
allele num: 118724
alternate allele: CATATG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+39_845+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+39_593+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+39_767+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+39_845+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+39_686+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+39_845+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+39_845+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+39_686+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+39_338+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+39_845+43dupCATAT
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3199
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-240977973-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977973
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977973
    reference: chr 1
allele count: 1
allele frequency: 8.417366710998132e-6
allele num: 118802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+43T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+43T>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4093
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-240977975-ATGAAATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977975
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977968
    reference: chr 1
allele count: 1
allele frequency: 8.41651657212113e-6
allele num: 118814
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+34_845+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+34_767+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+34_338+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+34_845+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+34_845+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+34_845+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+34_686+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+34_593+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+34_845+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+34_686+40delAATTTCA
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12153
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: ATGAAATT
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS

1-240977976-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977976
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977976
    reference: chr 1
allele count: 1
allele frequency: 8.414533582403528e-6
allele num: 118842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+40A>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+40A>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

1-240977984-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977984
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977984
    reference: chr 1
allele count: 221
allele frequency: 1.854680340388392e-3
allele num: 119158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+32A>T
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+32A>T
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 15827
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 4
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

1-240977992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977992
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977992
    reference: chr 1
allele count: 1
allele frequency: 8.344041519950603e-6
allele num: 119846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+24T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+24T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11762
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3384
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

1-240977995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977995
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977995
    reference: chr 1
allele count: 6
allele frequency: 4.99425660490436e-5
allele num: 120138
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+21G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+21G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9642
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-240977999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240977999
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240977999
    reference: chr 1
allele count: 4
allele frequency: 3.321541859731287e-5
allele num: 120426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+17G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+17G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17258
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11859
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

1-240978001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978001
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978001
    reference: chr 1
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+15G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+15G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-240978005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978005
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978005
    reference: chr 1
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+11C>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+11C>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-240978006-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978006
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978006
    reference: chr 1
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+10T>G
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+10T>G
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-240978011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978011
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978011
    reference: chr 1
allele count: 1
allele frequency: 8.27841981522567e-6
allele num: 120796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+5G>A
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+5G>A
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: c.845+5G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

1-240978014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978014
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978014
    reference: chr 1
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.845+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.338+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.686+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.845+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.845+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.845+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.686+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.593+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.767+2T>C
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.845+2T>C
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9783
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: c.845+2T>C
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

1-240978018-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978018
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978018
    reference: chr 1
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.765C>A
  hgvsp: ENSP00000331485.7:p.Asp255Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.843C>A
  hgvsp: ENSP00000355521.1:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.843C>A
  hgvsp: ENSP00000384428.1:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.591C>A
  hgvsp: ENSP00000390138.2:p.Asp197Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.843C>A
  hgvsp: ENSP00000355522.1:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.843C>A
  hgvsp: ENSP00000355520.4:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.684C>A
  hgvsp: ENSP00000341242.2:p.Asp228Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.336C>A
  hgvsp: ENSP00000404399.1:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.684C>A
  hgvsp: ENSP00000385508.1:p.Asp228Glu
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.843C>A
  hgvsp: ENSP00000355523.1:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp281Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

1-240978020-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978020
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978020
    reference: chr 1
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.841G>C
  hgvsp: ENSP00000355523.1:p.Asp281His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.763G>C
  hgvsp: ENSP00000331485.7:p.Asp255His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.334G>C
  hgvsp: ENSP00000404399.1:p.Asp112His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.682G>C
  hgvsp: ENSP00000341242.2:p.Asp228His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.841G>C
  hgvsp: ENSP00000384428.1:p.Asp281His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.841G>C
  hgvsp: ENSP00000355521.1:p.Asp281His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.682G>C
  hgvsp: ENSP00000385508.1:p.Asp228His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.589G>C
  hgvsp: ENSP00000390138.2:p.Asp197His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.841G>C
  hgvsp: ENSP00000355522.1:p.Asp281His
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.841G>C
  hgvsp: ENSP00000355520.4:p.Asp281His
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp281His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-240978023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978023
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978023
    reference: chr 1
allele count: 7
allele frequency: 5.782352260899734e-5
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.586G>A
  hgvsp: ENSP00000390138.2:p.Ala196Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.838G>A
  hgvsp: ENSP00000355520.4:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.838G>A
  hgvsp: ENSP00000355523.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.679G>A
  hgvsp: ENSP00000385508.1:p.Ala227Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.838G>A
  hgvsp: ENSP00000355522.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.679G>A
  hgvsp: ENSP00000341242.2:p.Ala227Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.838G>A
  hgvsp: ENSP00000355521.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.838G>A
  hgvsp: ENSP00000384428.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.760G>A
  hgvsp: ENSP00000331485.7:p.Ala254Thr
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.331G>A
  hgvsp: ENSP00000404399.1:p.Ala111Thr
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala280Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

1-240978026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978026
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978026
    reference: chr 1
allele count: 3
allele frequency: 2.477291494632535e-5
allele num: 121100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.835G>A
  hgvsp: ENSP00000384428.1:p.Val279Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.676G>A
  hgvsp: ENSP00000385508.1:p.Val226Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.835G>A
  hgvsp: ENSP00000355520.4:p.Val279Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.835G>A
  hgvsp: ENSP00000355523.1:p.Val279Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.835G>A
  hgvsp: ENSP00000355522.1:p.Val279Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.583G>A
  hgvsp: ENSP00000390138.2:p.Val195Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.676G>A
  hgvsp: ENSP00000341242.2:p.Val226Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.328G>A
  hgvsp: ENSP00000404399.1:p.Val110Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.835G>A
  hgvsp: ENSP00000355521.1:p.Val279Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.757G>A
  hgvsp: ENSP00000331485.7:p.Val253Ile
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val279Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS

1-240978027-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978027
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978027
    reference: chr 1
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.675A>G
  hgvsp: ENST00000348120.2:c.675A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.834A>G
  hgvsp: ENST00000366564.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.834A>G
  hgvsp: ENST00000407727.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.756A>G
  hgvsp: ENST00000331110.7:c.756A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.834A>G
  hgvsp: ENST00000366565.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.834A>G
  hgvsp: ENST00000366562.4:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.834A>G
  hgvsp: ENST00000366563.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.582A>G
  hgvsp: ENST00000446183.2:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.327A>G
  hgvsp: ENST00000440928.1:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.675A>G
  hgvsp: ENST00000401882.1:c.675A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys278Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

1-240978041-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978041
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978041
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.820T>A
  hgvsp: ENSP00000355522.1:p.Leu274Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.820T>A
  hgvsp: ENSP00000355521.1:p.Leu274Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.820T>A
  hgvsp: ENSP00000355520.4:p.Leu274Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.661T>A
  hgvsp: ENSP00000341242.2:p.Leu221Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.820T>A
  hgvsp: ENSP00000355523.1:p.Leu274Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.313T>A
  hgvsp: ENSP00000404399.1:p.Leu105Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.661T>A
  hgvsp: ENSP00000385508.1:p.Leu221Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.742T>A
  hgvsp: ENSP00000331485.7:p.Leu248Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.568T>A
  hgvsp: ENSP00000390138.2:p.Leu190Ile
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.820T>A
  hgvsp: ENSP00000384428.1:p.Leu274Ile
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu274Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-240978043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 240978043
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 240978043
    reference: chr 1
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000390138
  ensembl transcript: ENST00000446183
  gene symbol: RGS7
  hgvsc: ENST00000446183.2:c.566G>A
  hgvsp: ENSP00000390138.2:p.Arg189Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000331485
  ensembl transcript: ENST00000331110
  gene symbol: RGS7
  hgvsc: ENST00000331110.7:c.740G>A
  hgvsp: ENSP00000331485.7:p.Arg247Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355523
  ensembl transcript: ENST00000366565
  gene symbol: RGS7
  hgvsc: ENST00000366565.1:c.818G>A
  hgvsp: ENSP00000355523.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000384428
  ensembl transcript: ENST00000407727
  gene symbol: RGS7
  hgvsc: ENST00000407727.1:c.818G>A
  hgvsp: ENSP00000384428.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000404399
  ensembl transcript: ENST00000440928
  gene symbol: RGS7
  hgvsc: ENST00000440928.1:c.311G>A
  hgvsp: ENSP00000404399.1:p.Arg104Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355521
  ensembl transcript: ENST00000366563
  gene symbol: RGS7
  hgvsc: ENST00000366563.1:c.818G>A
  hgvsp: ENSP00000355521.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355522
  ensembl transcript: ENST00000366564
  gene symbol: RGS7
  hgvsc: ENST00000366564.1:c.818G>A
  hgvsp: ENSP00000355522.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000341242
  ensembl transcript: ENST00000348120
  gene symbol: RGS7
  hgvsc: ENST00000348120.2:c.659G>A
  hgvsp: ENSP00000341242.2:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000385508
  ensembl transcript: ENST00000401882
  gene symbol: RGS7
  hgvsc: ENST00000401882.1:c.659G>A
  hgvsp: ENSP00000385508.1:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/10003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182901
  ensembl protein: ENSP00000355520
  ensembl transcript: ENST00000366562
  gene symbol: RGS7
  hgvsc: ENST00000366562.4:c.818G>A
  hgvsp: ENSP00000355520.4:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/10003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg273Gln
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 3800
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2120
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2441
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43289
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1206
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1713
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.99199712256092e-5
allele num: 66726
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.319003e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

QD
type: SiteQuality
SIO_000300: 1.532e1

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2441
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43289
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3800
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

DP
type: SiteQuality
SIO_000300: 3.319003e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.532e1

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

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1208
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1713
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43284
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3191
bin: 9.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.126e0

QD
type: SiteQuality
SIO_000300: 1.253e1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

DP
type: SiteQuality
SIO_000300: 3.318735e6

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

GenotypeQuality
all individuals: 1710
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3192
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2825
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
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SIO_000300: -1.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
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SIO_000300: 1.816e0

MQRankSum
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SIO_000300: 4.08e-1

QD
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SIO_000300: 1.326e1

VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.65e-1

DP
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SIO_000300: 3.31854e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997422216893472e-5
allele num: 66724
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQ
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SIO_000300: 5.963e1

QD
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ReadPosRankSum
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SIO_000300: 1.32e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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FS
type: SiteQuality
SIO_000300: 1.574e0

MQ
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ClippingRankSum
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SIO_000300: 1.5e0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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Other
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
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SIO_000300: 6.26e-1

MQ
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SIO_000300: 5.973e1

BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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SIO_000300: 3.317852e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

Other
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allele num: 908
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8646
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 1.93e0

QD
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MQ
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

European (Finnish)
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allele num: 6610
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Other
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Latino
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South Asian
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East Asian
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DP
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VQSLOD
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BaseQRankSum
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MQ
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FS
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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European (Finnish)
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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Other
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European (Non-Finnish)
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QD
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MQ
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DP
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

South Asian
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allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
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European (Non-Finnish)
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allele count: 60
allele frequency: 8.99496282082034e-4
allele num: 66704
num of homozygotes: 0

East Asian
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allele count: 28
allele frequency: 3.239990742883592e-3
allele num: 8642
num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: 2.9e-1

InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 5.6e-2

DP
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SIO_000300: 3.316653e6

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 2.999e0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.62962962962963e-4
allele num: 8640
num of homozygotes: 0

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

BaseQRankSum
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DP
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MQRankSum
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SIO_000300: 2.8e-2

MQ
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ReadPosRankSum
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FS
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SIO_000300: 8.032e0

InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 3.48e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 1.387e0

DP
type: SiteQuality
SIO_000300: 3.311231e6

BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

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

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

African
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allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 3.31091e6

VQSLOD
type: SiteQuality
SIO_000300: -1.921e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.055e1

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 3.305431e6

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

African
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ReadPosRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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MQRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 3.305431e6

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999940001199976e-5
allele num: 66668
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 13
allele frequency: 1.967312348668281e-3
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Latino
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Other
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East Asian
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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FS
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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South Asian
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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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001200480192077e-5
allele num: 66640
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 2.061e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 3.299847e6

FS
type: SiteQuality
SIO_000300: 4.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

GenotypeQuality
all individuals: 467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3326
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4930
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13181
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6644
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.709608158883521e-5
allele num: 14904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.370054e6

FS
type: SiteQuality
SIO_000300: 2.414e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.697e0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6676
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16625
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2822
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 626
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6460
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6366
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6769
bin: 9.75e1
variant carriers: 48

South Asian
type: Population
allele count: 19
allele frequency: 1.268527173187341e-3
allele num: 14978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.734014558627525e-4
allele num: 58522
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.344447432105405e-4
allele num: 7438
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.096491228070175e-4
allele num: 9120
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: 6142
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.206757843925985e-3
allele num: 9944
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

QD
type: SiteQuality
SIO_000300: 1.424e1

DP
type: SiteQuality
SIO_000300: 1.393805e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 645
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26948
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6474
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variant carriers: 0

GenotypeQuality
all individuals: 3723
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 426
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variant carriers: 0

GenotypeQuality
all individuals: 223
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variant carriers: 0

GenotypeQuality
all individuals: 4919
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variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6738
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59474
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.163097555699762e-4
allele num: 9246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7534
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.475494e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5648
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 31402
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variant carriers: 0

GenotypeQuality
all individuals: 825
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variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
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variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6734
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 676
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60390
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.06700810926163e-4
allele num: 9372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.30582397492818e-4
allele num: 7658
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.533644e6

FS
type: SiteQuality
SIO_000300: 1.052e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.850000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.388e0

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeQuality
all individuals: 720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6747
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33278
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.643169345032699e-4
allele num: 60858
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.204819277108434e-3
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9434
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.585315408479835e-4
allele num: 7736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15286
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.554173e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 5.843e0

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
all individuals: 587
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
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variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
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GenotypeQuality
all individuals: 2345
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 361
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GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42035
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variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6738
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.552409339294585e-5
allele num: 64416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.719e0

MQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.348e0

DP
type: SiteQuality
SIO_000300: 1.663349e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.684e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3743
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6745
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
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GenotypeQuality
all individuals: 101
bin: 5.25e1
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GenotypeQuality
all individuals: 227
bin: 8.75e1
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GenotypeQuality
all individuals: 747
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.210067763794773e-4
allele num: 66112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.053e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

DP
type: SiteQuality
SIO_000300: 1.7104e6

QD
type: SiteQuality
SIO_000300: 1.139e1

FS
type: SiteQuality
SIO_000300: 7.196e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

GenotypeQuality
all individuals: 502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 771
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variant carriers: 0

GenotypeQuality
all individuals: 46155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6741
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.25e1
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GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 12
allele frequency: 7.352040191153045e-4
allele num: 16322
num of homozygotes: 1

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

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

Other
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allele num: 892
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FS
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 9.633911368015414e-5
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Latino
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European (Non-Finnish)
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allele num: 66620
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South Asian
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allele num: 16480
num of homozygotes: 0

European (Finnish)
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Other
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DP
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele num: 8648
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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DP
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VQSLOD
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FS
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66648
num of homozygotes: 0

East Asian
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African
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Other
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South Asian
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

European (Finnish)
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Other
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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African
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ClippingRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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Other
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African
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Latino
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European (Finnish)
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FS
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.156871818602499e-4
allele num: 8644
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South Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.929e1

ReadPosRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
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SIO_000300: 1.1779e1

MQRankSum
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SIO_000300: 2.22e-1

ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 1.840716652349982e-4
allele num: 16298
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66110
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African
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Other
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allele frequency: 0.0e0
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.153088850603002e-5
allele num: 16252
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 7.26e-1

DP
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 4.123e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.56e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.529239050648397e-5
allele num: 65392
num of homozygotes: 0

South Asian
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allele num: 16136
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

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

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

South Asian
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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Other
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East Asian
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InbreedingCoeff
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FS
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QD
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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Other
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European (Finnish)
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ReadPosRankSum
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.589324e6

VQSLOD
type: SiteQuality
SIO_000300: 4.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.55e-1

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61852
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15496
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

Latino
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allele frequency: 9.416195856873823e-5
allele num: 10620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

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

African
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allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.356380479291133e-5
allele num: 59588
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51970
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.060152499293985e-5
allele num: 14164
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.041e0

QD
type: SiteQuality
SIO_000300: 1.851e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

South Asian
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allele count: 2
allele frequency: 1.447387465624548e-4
allele num: 13818
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.093e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

DP
type: SiteQuality
SIO_000300: 1.199437e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535909565644775e-5
allele num: 65108
num of homozygotes: 0

Other
type: Population
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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FS
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 17
allele frequency: 2.609603340292275e-4
allele num: 65144
num of homozygotes: 0

Latino
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allele frequency: 8.742787200559538e-5
allele num: 11438
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 1.309955663039097e-3
allele num: 9924
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Other
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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FS
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MQ
type: SiteQuality
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.533836431682925e-5
allele num: 65196
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African
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East Asian
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European (Finnish)
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MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.797e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

DP
type: SiteQuality
SIO_000300: 2.072455e6

GenotypeQuality
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variant carriers: 1

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

African
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allele count: 1
allele frequency: 1.006238679814852e-4
allele num: 9938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65188
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.198e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.259e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.056e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.079324e6

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65212
num of homozygotes: 0

Latino
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allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.183e-1

ReadPosRankSum
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SIO_000300: -3.79e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 216

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65400
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.002807862013638e-4
allele num: 9972
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.746419839329375e-4
allele num: 11452
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

South Asian
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allele count: 217
allele frequency: 1.319148936170213e-2
allele num: 16450
num of homozygotes: 4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.474e0

FS
type: SiteQuality
SIO_000300: 8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

DP
type: SiteQuality
SIO_000300: 2.110955e6

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51846452866861e-5
allele num: 65856
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -1.146e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.654e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.129202e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

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

African
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allele count: 6
allele frequency: 5.938242280285036e-4
allele num: 10104
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.133e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.15e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.859e0

DP
type: SiteQuality
SIO_000300: 2.135392e6

MQRankSum
type: SiteQuality
SIO_000300: -4.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10156
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.038100413609878e-5
allele num: 66246
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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BaseQRankSum
type: SiteQuality
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MQ
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele num: 66314
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
allele num: 16480
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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DP
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.43e-1

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

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8584
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
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South Asian
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allele frequency: 6.066488716330988e-5
allele num: 16484
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QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506795648374167e-5
allele num: 66366
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 4.52e0

ReadPosRankSum
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SIO_000300: -1.274e0

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

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

FS
type: SiteQuality
SIO_000300: 1.354e0

MQRankSum
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SIO_000300: 2.33e0

VQSLOD
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SIO_000300: -2.336e0

DP
type: SiteQuality
SIO_000300: 2.144243e6

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

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

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

QD
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.32e0

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

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

Latino
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allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -1.057e0

InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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SIO_000300: 2.146518e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

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

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

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

South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.147591e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
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South Asian
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allele count: 0
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: 1.86e0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.512470701364265e-5
allele num: 66556
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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South Asian
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allele num: 16500
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DP
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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MQ
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SIO_000300: 5.973e1

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

European (Non-Finnish)
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allele num: 66590
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European (Finnish)
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African
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Other
type: Population
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Latino
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South Asian
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East Asian
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

African
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allele count: 0
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European (Finnish)
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allele num: 6606
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

QD
type: SiteQuality
SIO_000300: 1.505e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

DP
type: SiteQuality
SIO_000300: 2.149343e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

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

GenotypeQuality
all individuals: 16658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4422
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4969
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6166
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3431
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

FS
type: SiteQuality
SIO_000300: 6.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

VQSLOD
type: SiteQuality
SIO_000300: 5.570000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.150038e6