6-46991771-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991771
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991771
    reference: chr 6
allele count: 73
allele frequency: 6.28800799352249e-4
allele num: 116094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.476+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.221+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.503+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.422+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.313+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.484+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.451+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.451+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.404+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.255+9C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.516+9C>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35378
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

6-46991771-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991771
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991771
    reference: chr 6
allele count: 1
allele frequency: 8.613709580167795e-6
allele num: 116094
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.451+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.313+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.422+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.451+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.221+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.484+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.476+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.516+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.503+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.404+9C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.255+9C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41093
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

6-46991773-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991773
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991773
    reference: chr 6
allele count: 1
allele frequency: 8.590770076629668e-6
allele num: 116404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.476+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.503+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.451+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.313+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.516+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.221+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.484+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.255+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.422+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.404+7A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.451+7A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451+7A>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

6-46991774-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991774
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991774
    reference: chr 6
allele count: 2
allele frequency: 1.71556013038257e-5
allele num: 116580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.516+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.221+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.451+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.313+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.503+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.476+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.404+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.484+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.255+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.451+6C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.422+6C>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451+6C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

6-46991775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991775
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991775
    reference: chr 6
allele count: 2
allele frequency: 1.712827364129969e-5
allele num: 116766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.255+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.484+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.476+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.404+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.313+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.221+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.451+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.516+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.422+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.451+5G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.503+5G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451+5G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-46991792-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991792
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991792
    reference: chr 6
allele count: 2
allele frequency: 1.674621116972285e-5
allele num: 119430
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.439T>C
  hgvsp: ENSP00000360299.2:p.Cys147Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.209T>C
  hgvsp: ENSP00000419109.1:p.Cys71Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.464T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.472T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.392T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.243T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.504T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.301T>C
  hgvsp: ENSP00000417732.1:p.Cys101Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.410T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.439T>C
  hgvsp: ENSP00000360289.2:p.Cys147Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.491T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys147Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

6-46991803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991803
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991803
    reference: chr 6
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.461G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.493G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.428G>C
  hgvsp: ENSP00000360289.2:p.Ser143Thr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.198G>C
  hgvsp: ENSP00000419109.1:p.Ser67Thr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.290G>C
  hgvsp: ENSP00000417732.1:p.Ser97Thr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.232G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.381G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.428G>C
  hgvsp: ENSP00000360299.2:p.Ser143Thr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.453G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.399G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.480G>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser143Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

6-46991807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991807
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991807
    reference: chr 6
allele count: 10
allele frequency: 8.297102651754008e-5
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.194C>T
  hgvsp: ENSP00000419109.1:p.Gln66Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.424C>T
  hgvsp: ENSP00000360299.2:p.Gln142Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.286C>T
  hgvsp: ENSP00000417732.1:p.Gln96Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.424C>T
  hgvsp: ENSP00000360289.2:p.Gln142Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.457C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.449C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.476C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.395C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.228C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.377C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.489C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln142Ter
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

6-46991815-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991815
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991815
    reference: chr 6
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.186A>G
  hgvsp: ENSP00000419109.1:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.278A>G
  hgvsp: ENSP00000417732.1:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.449A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.481A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.468A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.416A>G
  hgvsp: ENSP00000360289.2:p.Asn139Ser
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.220A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.416A>G
  hgvsp: ENSP00000360299.2:p.Asn139Ser
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.387A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.441A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.369A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn139Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

6-46991820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991820
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991820
    reference: chr 6
allele count: 4
allele frequency: 3.307261091726886e-5
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.476C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.444C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.215C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.411C>T
  hgvsp: ENST00000371253.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.273C>T
  hgvsp: ENST00000475745.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.364C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.463C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.436C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.411C>T
  hgvsp: ENST00000371243.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.181C>T
  hgvsp: ENST00000487323.1:c.181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.382C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu137Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

6-46991824-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991824
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991824
    reference: chr 6
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.472A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.440A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.269A>C
  hgvsp: ENSP00000417732.1:p.His90Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.407A>C
  hgvsp: ENSP00000360289.2:p.His136Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.407A>C
  hgvsp: ENSP00000360299.2:p.His136Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.432A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.211A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.360A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.378A>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.177A>C
  hgvsp: ENSP00000419109.1:p.His60Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.459A>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His136Pro
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-46991837-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991837
    reference: chr 6
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.365A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.347A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.419A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.427A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.394A>G
  hgvsp: ENSP00000360299.2:p.Ser132Gly
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.256A>G
  hgvsp: ENSP00000417732.1:p.Ser86Gly
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.198A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.459A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.164A>G
  hgvsp: ENSP00000419109.1:p.Ser56Gly
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.394A>G
  hgvsp: ENSP00000360289.2:p.Ser132Gly
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.446A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser132Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-46991841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991841
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991841
    reference: chr 6
allele count: 3
allele frequency: 2.477046040029064e-5
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.390C>T
  hgvsp: ENST00000371243.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.415C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.361C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.252C>T
  hgvsp: ENST00000475745.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.455C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.390C>T
  hgvsp: ENST00000371253.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.194C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.423C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.343C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.160C>T
  hgvsp: ENST00000487323.1:c.160C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.442C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu130Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

6-46991844-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991844
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991844
    reference: chr 6
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.249A>G
  hgvsp: ENST00000475745.1:c.249A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.452A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.157A>G
  hgvsp: ENST00000487323.1:c.157A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.412A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.387A>G
  hgvsp: ENST00000371253.2:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.420A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.358A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.439A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.340A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.387A>G
  hgvsp: ENST00000371243.2:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.191A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala129Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-46991853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991853
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991853
    reference: chr 6
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.411G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.331G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.378G>A
  hgvsp: ENST00000371253.2:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.182G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.443G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.240G>A
  hgvsp: ENST00000475745.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.430G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.148G>A
  hgvsp: ENST00000487323.1:c.148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.349G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.378G>A
  hgvsp: ENST00000371243.2:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.403G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr126Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-46991854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991854
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991854
    reference: chr 6
allele count: 5
allele frequency: 4.127864738128261e-5
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.147C>T
  hgvsp: ENSP00000419109.1:p.Thr50Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.402C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.330C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.442C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.429C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.239C>T
  hgvsp: ENSP00000417732.1:p.Thr80Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.181C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.410C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.377C>T
  hgvsp: ENSP00000360289.2:p.Thr126Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.377C>T
  hgvsp: ENSP00000360299.2:p.Thr126Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.348C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr126Met
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

6-46991860-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991860
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991860
    reference: chr 6
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.371T>C
  hgvsp: ENSP00000360299.2:p.Leu124Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.371T>C
  hgvsp: ENSP00000360289.2:p.Leu124Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.436T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.324T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.423T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.233T>C
  hgvsp: ENSP00000417732.1:p.Leu78Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.404T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.175T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.141T>C
  hgvsp: ENSP00000419109.1:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.396T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.342T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu124Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-46991860-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991860
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991860
    reference: chr 6
allele count: 3
allele frequency: 2.476228209191759e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.342T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.423T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.175T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.436T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.371T>A
  hgvsp: ENSP00000360289.2:p.Leu124His
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.233T>A
  hgvsp: ENSP00000417732.1:p.Leu78His
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.404T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.141T>A
  hgvsp: ENSP00000419109.1:p.Leu48His
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.371T>A
  hgvsp: ENSP00000360299.2:p.Leu124His
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.324T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.396T>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu124His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

6-46991862-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991862
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991862
    reference: chr 6
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.421C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.322C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.231C>A
  hgvsp: ENSP00000417732.1:p.Tyr77Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.369C>A
  hgvsp: ENSP00000360299.2:p.Tyr123Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.434C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.173C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.139C>A
  hgvsp: ENSP00000419109.1:p.Tyr47Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.394C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.340C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.402C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.369C>A
  hgvsp: ENSP00000360289.2:p.Tyr123Ter
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr123Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-46991866-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991866
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991866
    reference: chr 6
allele count: 2
allele frequency: 1.650709805216243e-5
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.135G>T
  hgvsp: ENSP00000419109.1:p.Cys46Phe
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.398G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.169G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.365G>T
  hgvsp: ENSP00000360299.2:p.Cys122Phe
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.365G>T
  hgvsp: ENSP00000360289.2:p.Cys122Phe
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.227G>T
  hgvsp: ENSP00000417732.1:p.Cys76Phe
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.318G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.390G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.430G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.336G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.417G>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys122Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-46991871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991871
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991871
    reference: chr 6
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.360G>A
  hgvsp: ENST00000371253.2:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.385G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.313G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.331G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.222G>A
  hgvsp: ENST00000475745.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.412G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.360G>A
  hgvsp: ENST00000371243.2:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.164G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.130G>A
  hgvsp: ENST00000487323.1:c.130G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.393G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.425G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln120Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

6-46991875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991875
    reference: chr 6
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.327C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.389C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.218C>T
  hgvsp: ENSP00000417732.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.421C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.126C>T
  hgvsp: ENSP00000419109.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.356C>T
  hgvsp: ENSP00000360289.2:p.Pro119Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.408C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.381C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.160C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.356C>T
  hgvsp: ENSP00000360299.2:p.Pro119Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.309C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro119Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-46991876-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991876
    reference: chr 6
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.308C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.159C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.125C>G
  hgvsp: ENSP00000419109.1:p.Pro43Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.407C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.326C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.355C>G
  hgvsp: ENSP00000360299.2:p.Pro119Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.420C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.380C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.355C>G
  hgvsp: ENSP00000360289.2:p.Pro119Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.217C>G
  hgvsp: ENSP00000417732.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.388C>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro119Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

6-46991876-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991875
    reference: chr 6
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.419delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.354delT
  hgvsp: ENSP00000360299.2:p.Gln120ArgfsTer48
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.307delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.158delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.216delT
  hgvsp: ENSP00000417732.1:p.Gln74ArgfsTer48
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.325delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.354delT
  hgvsp: ENSP00000360289.2:p.Gln120ArgfsTer48
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.406delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.124delT
  hgvsp: ENSP00000419109.1:p.Gln44ArgfsTer48
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.387delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.379delT
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln120ArgfsTer48
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: GA
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

6-46991881-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991881
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991881
    reference: chr 6
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.415T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.350T>C
  hgvsp: ENSP00000360289.2:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.350T>C
  hgvsp: ENSP00000360299.2:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.383T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.402T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.120T>C
  hgvsp: ENSP00000419109.1:p.Leu41Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.321T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.212T>C
  hgvsp: ENSP00000417732.1:p.Leu71Pro
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.154T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.303T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.375T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu117Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

6-46991886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991886
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991886
    reference: chr 6
allele count: 2
allele frequency: 1.651200422707308e-5
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.298A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.345A>G
  hgvsp: ENST00000371243.2:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.345A>G
  hgvsp: ENST00000371253.2:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.149A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.397A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.115A>G
  hgvsp: ENST00000487323.1:c.115A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.370A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.207A>G
  hgvsp: ENST00000475745.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.378A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.316A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.410A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser115Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

6-46991905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991905
    reference: chr 6
allele count: 3
allele frequency: 2.479830710223515e-5
allele num: 120976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.326A>G
  hgvsp: ENSP00000360289.2:p.Tyr109Cys
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.326A>G
  hgvsp: ENSP00000360299.2:p.Tyr109Cys
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.351A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.378A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.96A>G
  hgvsp: ENSP00000419109.1:p.Tyr33Cys
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.279A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.359A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.188A>G
  hgvsp: ENSP00000417732.1:p.Tyr63Cys
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.130A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.297A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.391A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr109Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-46991923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991923
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991923
    reference: chr 6
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.112G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.308G>A
  hgvsp: ENSP00000360289.2:p.Cys103Tyr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.341G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.308G>A
  hgvsp: ENSP00000360299.2:p.Cys103Tyr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.170G>A
  hgvsp: ENSP00000417732.1:p.Cys57Tyr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.360G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.373G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.78G>A
  hgvsp: ENSP00000419109.1:p.Cys27Tyr
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.261G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.279G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.333G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys103Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

6-46991932-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991932
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991932
    reference: chr 6
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.252T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.270T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.351T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.69T>C
  hgvsp: ENSP00000419109.1:p.Val24Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.103T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.299T>C
  hgvsp: ENSP00000360299.2:p.Val100Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.161T>C
  hgvsp: ENSP00000417732.1:p.Val54Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.299T>C
  hgvsp: ENSP00000360289.2:p.Val100Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.332T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.364T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.324T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val100Ala
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-46991936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991936
    reference: chr 6
allele count: 1
allele frequency: 8.338475393159114e-6
allele num: 119926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.360G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.65G>A
  hgvsp: ENSP00000419109.1:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.320G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.99G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.347G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.295G>A
  hgvsp: ENSP00000360299.2:p.Gly99Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.266G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.157G>A
  hgvsp: ENSP00000417732.1:p.Gly53Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.248G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.295G>A
  hgvsp: ENSP00000360289.2:p.Gly99Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.328G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly99Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

6-46991942-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991942
    reference: chr 6
allele count: 2
allele frequency: 1.673080140538732e-5
allele num: 119540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.314C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.151C>A
  hgvsp: ENSP00000417732.1:p.Leu51Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.289C>A
  hgvsp: ENSP00000360299.2:p.Leu97Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.260C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.242C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.289C>A
  hgvsp: ENSP00000360289.2:p.Leu97Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.59C>A
  hgvsp: ENSP00000419109.1:p.Leu21Met
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.322C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.354C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.341C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.93C>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu97Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

6-46991943-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991943
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991943
    reference: chr 6
allele count: 277
allele frequency: 2.317060929501121e-3
allele num: 119548
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.288C>G
  hgvsp: ENSP00000360299.2:p.Ser96Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.150C>G
  hgvsp: ENSP00000417732.1:p.Ser50Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.58C>G
  hgvsp: ENSP00000419109.1:p.Ser20Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.288C>G
  hgvsp: ENSP00000360289.2:p.Ser96Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.321C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.353C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.241C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.92C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.313C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.340C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.259C>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14142
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 34553
  bin: 2.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
hgvs: p.Ser96Arg
num of homozygotes: 5
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

6-46991946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991946
    reference: chr 6
allele count: 1
allele frequency: 8.382229673093043e-6
allele num: 119300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.337C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.147C>T
  hgvsp: ENST00000475745.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.89C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.350C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.310C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.238C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.55C>T
  hgvsp: ENST00000487323.1:c.55C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.285C>T
  hgvsp: ENST00000371243.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.285C>T
  hgvsp: ENST00000371253.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.256C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.318C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn95Asn
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-46991959-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991959
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991959
    reference: chr 6
allele count: 5
allele frequency: 4.226042564700711e-5
allele num: 118314
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.76G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-6G>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-6G>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.278-6G>C
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

6-46991960-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991960
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991960
    reference: chr 6
allele count: 1
allele frequency: 8.453799983092399e-6
allele num: 118290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.75T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-7T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-7T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.278-7T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-46991962-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991962
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991961
    reference: chr 6
allele count: 51
allele frequency: 4.313698954562371e-4
allele num: 118228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.72delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-10delT
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-10delT
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32519
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: GA
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-46991964-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991964
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991964
    reference: chr 6
allele count: 1
allele frequency: 8.479318941102651e-6
allele num: 117934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.71T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-11T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-11T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

6-46991968-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991968
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991968
    reference: chr 6
allele count: 1
allele frequency: 8.486514927779759e-6
allele num: 117834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.67C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-15C>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-15C>A
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/6-46991969-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991969
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991969
    reference: chr 6
allele count: 1
allele frequency: 8.489396743467409e-6
allele num: 117794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.66T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-16T>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-16T>G
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30735
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

6-46991972-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991972
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991971
    reference: chr 6
allele count: 42
allele frequency: 3.571975302342195e-4
allele num: 117582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-20delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.62delG
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29535
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TC
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-46991976-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991976
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991976
    reference: chr 6
allele count: 75
allele frequency: 6.403579173852906e-4
allele num: 117122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.59A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-23A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-23A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11667
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26250
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

6-46991993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46991993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46991993
    reference: chr 6
allele count: 1
allele frequency: 8.621878879845495e-6
allele num: 115984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.231-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.140-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.303-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000493249
  gene symbol: GPR110
  hgvsc: ENST00000493249.1:n.42A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.278-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.343-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.249-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.48-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.330-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.278-40A>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.311-40A>T
  variant of: http://identifiers.org/hgnc/18990
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3259
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

6-46993545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993545
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993545
    reference: chr 6
allele count: 728
allele frequency: 6.274239420839438e-3
allele num: 116030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+45G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+45G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 6.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 7804
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 6.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 8.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 9.75e1
  variant carriers: 199
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 34
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-46993546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993546
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993546
    reference: chr 6
allele count: 1
allele frequency: 8.619352169490942e-6
allele num: 116018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+44G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+44G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/6-46993547-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993547
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993547
    reference: chr 6
allele count: 1
allele frequency: 8.611335962661248e-6
allele num: 116126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+43G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+43G>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

6-46993547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993547
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993547
    reference: chr 6
allele count: 3
allele frequency: 2.583400788798374e-5
allele num: 116126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+43G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+43G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-46993548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993548
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993548
    reference: chr 6
allele count: 8
allele frequency: 6.888238333046323e-5
allele num: 116140
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+42C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+42C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24393
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-46993552-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993552
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993551
    reference: chr 6
allele count: 1
allele frequency: 8.584870025067821e-6
allele num: 116484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+37delG
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+37delG
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24390
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: TC
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

6-46993562-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993562
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993562
    reference: chr 6
allele count: 468
allele frequency: 4.002805384970663e-3
allele num: 116918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+28A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+28A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 9.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 1.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 7
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-46993566-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993566
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993566
    reference: chr 6
allele count: 1
allele frequency: 8.541460248044005e-6
allele num: 117076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+24A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+24A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5012
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

6-46993575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993575
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993575
    reference: chr 6
allele count: 4
allele frequency: 3.396393030601501e-5
allele num: 117772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+15G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+15G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

6-46993576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993576
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993576
    reference: chr 6
allele count: 30
allele frequency: 2.539618041446567e-4
allele num: 118128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+14C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+14C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24237
  bin: 9.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

6-46993580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993580
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993580
    reference: chr 6
allele count: 1
allele frequency: 8.442095665828085e-6
allele num: 118454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+10C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+10C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12218
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

6-46993581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993581
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993581
    reference: chr 6
allele count: 4
allele frequency: 3.375926269770268e-5
allele num: 118486
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+9G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+9G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3524
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/6-46993582-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993582
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993582
    reference: chr 6
allele count: 1
allele frequency: 8.426303549159055e-6
allele num: 118676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.47+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.230+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.310+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.277+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.139+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.302+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.248+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.277+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.329+8G>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.342+8G>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3921
  bin: 8.25e1
  variant carriers: 0
hgvs: c.277+8G>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-46993594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993594
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993594
    reference: chr 6
allele count: 3
allele frequency: 2.508822693137534e-5
allele num: 119578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.325C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.226C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.338C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.306C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.43C>T
  hgvsp: ENST00000487323.1:c.43C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.273C>T
  hgvsp: ENST00000371253.2:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.273C>T
  hgvsp: ENST00000371243.2:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.244C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.298C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.135C>T
  hgvsp: ENST00000475745.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr91Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-46993598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993598
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993598
    reference: chr 6
allele count: 1
allele frequency: 8.343484572897024e-6
allele num: 119854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.321C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.39C>T
  hgvsp: ENSP00000419109.1:p.Ala14Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.131C>T
  hgvsp: ENSP00000417732.1:p.Ala44Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.269C>T
  hgvsp: ENSP00000360289.2:p.Ala90Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.222C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.334C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.240C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.302C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.269C>T
  hgvsp: ENSP00000360299.2:p.Ala90Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.294C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala90Val
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

6-46993618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993618
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993618
    reference: chr 6
allele count: 2
allele frequency: 1.654670306941342e-5
allele num: 120870
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.249T>C
  hgvsp: ENST00000371253.2:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.19T>C
  hgvsp: ENST00000487323.1:c.19T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.111T>C
  hgvsp: ENST00000475745.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.282T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.274T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.220T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.249T>C
  hgvsp: ENST00000371243.2:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.314T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.202T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.301T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3524
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile83Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-46993620-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993620
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993620
    reference: chr 6
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.218A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.280A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.299A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.109A>G
  hgvsp: ENSP00000417732.1:p.Ile37Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.247A>G
  hgvsp: ENSP00000360299.2:p.Ile83Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.312A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.17A>G
  hgvsp: ENSP00000419109.1:p.Ile7Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.247A>G
  hgvsp: ENSP00000360289.2:p.Ile83Val
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.200A>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.272A>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14523
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3919
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile83Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

6-46993623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993623
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993623
    reference: chr 6
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.269C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.14C>T
  hgvsp: ENST00000487323.1:c.14C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.309C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.277C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.197C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.244C>T
  hgvsp: ENST00000371243.2:c.244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.215C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.244C>T
  hgvsp: ENST00000371253.2:c.244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.296C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.106C>T
  hgvsp: ENST00000475745.1:c.106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu82Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-46993631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993631
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993631
    reference: chr 6
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.207C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.6C>T
  hgvsp: ENSP00000419109.1:p.Ser3Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.236C>T
  hgvsp: ENSP00000360299.2:p.Ser79Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.236C>T
  hgvsp: ENSP00000360289.2:p.Ser79Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.269C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.189C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.288C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.261C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.98C>T
  hgvsp: ENSP00000417732.1:p.Ser33Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.301C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2439
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser79Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-46993634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993634
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993634
    reference: chr 6
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.233G>A
  hgvsp: ENSP00000360289.2:p.Trp78Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.95G>A
  hgvsp: ENSP00000417732.1:p.Trp32Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.258G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.204G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.3G>A
  hgvsp: ENSP00000419109.1:p.Trp2Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.298G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.285G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.266G>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.233G>A
  hgvsp: ENSP00000360299.2:p.Trp78Ter
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.186G>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4065
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Trp78Ter
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-46993635-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993635
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993635
    reference: chr 6
allele count: 10
allele frequency: 8.262687356435808e-5
allele num: 121026
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.232T>C
  hgvsp: ENSP00000360299.2:p.Trp78Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000419109
  ensembl transcript: ENST00000487323
  gene symbol: GPR110
  hgvsc: ENST00000487323.1:c.2T>C
  hgvsp: ENSP00000419109.1:p.Trp2Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.185T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.257T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.232T>C
  hgvsp: ENSP00000360289.2:p.Trp78Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.94T>C
  hgvsp: ENSP00000417732.1:p.Trp32Arg
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.297T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.265T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.284T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.203T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Trp78Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

6-46993641-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993641
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993641
    reference: chr 6
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.226T>A
  hgvsp: ENSP00000360299.2:p.Leu76Ile
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.88T>A
  hgvsp: ENSP00000417732.1:p.Leu30Ile
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.226T>A
  hgvsp: ENSP00000360289.2:p.Leu76Ile
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.197T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.179T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.259T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.278T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.251T>A
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.291T>A
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu76Ile
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-46993643-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993643
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993643
    reference: chr 6
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.195C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.289C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.224C>T
  hgvsp: ENSP00000360299.2:p.Pro75Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.276C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.177C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.86C>T
  hgvsp: ENSP00000417732.1:p.Pro29Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.224C>T
  hgvsp: ENSP00000360289.2:p.Pro75Leu
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.257C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.249C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro75Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

6-46993644-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993644
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993644
    reference: chr 6
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.85C>G
  hgvsp: ENSP00000417732.1:p.Pro29Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.275C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.288C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.223C>G
  hgvsp: ENSP00000360289.2:p.Pro75Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.256C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.194C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.248C>G
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.223C>G
  hgvsp: ENSP00000360299.2:p.Pro75Ala
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.176C>G
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14584
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro75Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

6-46993653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993653
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993653
    reference: chr 6
allele count: 134
allele frequency: 1.108409019471603e-3
allele num: 120894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.239T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.214T>C
  hgvsp: ENST00000371243.2:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.76T>C
  hgvsp: ENST00000475745.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.167T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.185T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.279T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.214T>C
  hgvsp: ENST00000371253.2:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.247T>C
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.266T>C
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu72Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

6-46993654-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46993654
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 46993654
    reference: chr 6
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000417732
  ensembl transcript: ENST00000475745
  gene symbol: GPR110
  hgvsc: ENST00000475745.1:c.75C>T
  hgvsp: ENST00000475745.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360289
  ensembl transcript: ENST00000371243
  gene symbol: GPR110
  hgvsc: ENST00000371243.2:c.213C>T
  hgvsp: ENST00000371243.2:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000419892
  gene symbol: GPR110
  hgvsc: ENST00000419892.2:n.265C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000474800
  gene symbol: GPR110
  hgvsc: ENST00000474800.1:n.238C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000449332
  gene symbol: GPR110
  hgvsc: ENST00000449332.2:n.184C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000471487
  gene symbol: GPR110
  hgvsc: ENST00000471487.1:n.246C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153292
  ensembl protein: ENSP00000360299
  ensembl transcript: ENST00000371253
  gene symbol: GPR110
  hgvsc: ENST00000371253.2:c.213C>T
  hgvsp: ENST00000371253.2:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000477771
  gene symbol: GPR110
  hgvsc: ENST00000477771.1:n.278C>T
  variant of: http://identifiers.org/hgnc/18990
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153292
  ensembl transcript: ENST00000491283
  gene symbol: GPR110
  hgvsc: ENST00000491283.1:n.166C>T
  variant of: http://identifiers.org/hgnc/18990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu71Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

GenotypeQuality
all individuals: 1269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3358
bin: 9.75e1
variant carriers: 72

GenotypeQuality
all individuals: 41093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64892
num of homozygotes: 0

African
type: Population
allele count: 70
allele frequency: 6.817296455005843e-3
allele num: 10268
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13826
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.674750356633381e-4
allele num: 11216
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

DP
type: SiteQuality
SIO_000300: 1.519518e6

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 850
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541022005794243e-5
allele num: 64892
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13826
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

DP
type: SiteQuality
SIO_000300: 1.519518e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeDepth
all individuals: 382
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65020
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.164350193437455e-5
allele num: 13958
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.63e1

DP
type: SiteQuality
SIO_000300: 1.524701e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 259
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 643
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14034
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.945525291828794e-4
allele num: 10280
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.52997e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

FS
type: SiteQuality
SIO_000300: 2.418e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 1.159e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.218e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeDepth
all individuals: 405
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3302
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14096
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068802553243724e-5
allele num: 65172
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.533817e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 8.938000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: -5.901999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

GenotypeQuality
all individuals: 5339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.326122354035822e-4
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.484e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.503e0

MQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

QD
type: SiteQuality
SIO_000300: 7.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.576232e6

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506841058405159e-5
allele num: 66364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.053e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.589995e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 9.42e0

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

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

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3310
bin: 9.75e1
variant carriers: 10

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 10
allele frequency: 6.194251734390486e-4
allele num: 16144
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.144e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

FS
type: SiteQuality
SIO_000300: 5.211e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.593788e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.6e0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46699
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1370
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
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variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.662e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.186999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.599228e6

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

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 367
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GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.886280546469117e-4
allele num: 10394
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.16e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: -6.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.165e0

FS
type: SiteQuality
SIO_000300: 2.745e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

DP
type: SiteQuality
SIO_000300: 1.600996e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1383
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.095330976472023e-5
allele num: 16406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.601792e6

QD
type: SiteQuality
SIO_000300: 1.051e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 7.555e0

MQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -1.196e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 5571
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.783e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 8.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.848e1

DP
type: SiteQuality
SIO_000300: 1.604304e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 56
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

South Asian
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allele count: 3
allele frequency: 1.82370820668693e-4
allele num: 16450
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.3e-3

ReadPosRankSum
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QD
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.604874e6

ClippingRankSum
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SIO_000300: 2.1e-2

FS
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BaseQRankSum
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SIO_000300: -1.512e0

MQRankSum
type: SiteQuality
SIO_000300: 6.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
all individuals: 75
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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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bin: 9.75e1
variant carriers: 1

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

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

Latino
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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: 8624
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 1.81e0

ClippingRankSum
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SIO_000300: -5.69e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.301e1

VQSLOD
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SIO_000300: 2.76e0

DP
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MQRankSum
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SIO_000300: -1.9e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-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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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.393e-1

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 5.785e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
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SIO_000300: 3.88e-1

DP
type: SiteQuality
SIO_000300: 1.60625e6

QD
type: SiteQuality
SIO_000300: 1.489e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

South Asian
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allele count: 5
allele frequency: 3.038405444822557e-4
allele num: 16456
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 2.6e-3

DP
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SIO_000300: 1.606672e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 1.091e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
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SIO_000300: 6.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
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 count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
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FS
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.271e1

InbreedingCoeff
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SIO_000300: 3.0e-3

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500855162480871e-5
allele num: 66654
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16460
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MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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SIO_000300: 1.271e1

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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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

East Asian
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allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 9.83e0

DP
type: SiteQuality
SIO_000300: 1.607003e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -3.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

East Asian
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allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.606992e6

ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 4.632e0

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

MQRankSum
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SIO_000300: -6.18e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
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SIO_000300: -1.68e-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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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: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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South Asian
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allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.81e-1

FS
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SIO_000300: 1.879e0

DP
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SIO_000300: 1.60717e6

ReadPosRankSum
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SIO_000300: 8.699999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.49e-1

QD
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SIO_000300: 7.71e0

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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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
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 frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

InbreedingCoeff
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BaseQRankSum
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FS
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QD
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SIO_000300: 1.2e1

MQRankSum
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ClippingRankSum
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SIO_000300: -2.61e-1

ReadPosRankSum
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SIO_000300: -2.37e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.607127e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

Other
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allele num: 906
num of homozygotes: 0

South Asian
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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DP
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BaseQRankSum
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SIO_000300: -6.870000000000001e-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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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

DP
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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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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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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 3.001741009785676e-5
allele num: 66628
num of homozygotes: 0

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

Other
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allele count: 0
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.219363492257042e-4
allele num: 16402
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11494
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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QD
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FS
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e0

DP
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BaseQRankSum
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ClippingRankSum
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FS
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SIO_000300: 2.22e0

VQSLOD
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SIO_000300: -3.815e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQRankSum
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SIO_000300: -6.01e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.047e1

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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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15978
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
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VQSLOD
type: SiteQuality
SIO_000300: -1.274e0

MQRankSum
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SIO_000300: -1.583e0

MQ
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SIO_000300: 5.944e1

ReadPosRankSum
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SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 5.159e0

DP
type: SiteQuality
SIO_000300: 1.586617e6

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

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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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

African
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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: 15856
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.59e0

ClippingRankSum
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SIO_000300: 2.07e-1

QD
type: SiteQuality
SIO_000300: 2.276e1

InbreedingCoeff
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SIO_000300: 6.4e-3

MQ
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SIO_000300: 5.957e1

VQSLOD
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SIO_000300: -1.886e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.83e-1

MQRankSum
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SIO_000300: 3.29e-1

DP
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SIO_000300: 1.582664e6

BaseQRankSum
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SIO_000300: -1.497e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.02571860816944e-5
allele num: 66100
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.3e-2

BaseQRankSum
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SIO_000300: -6.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

DP
type: SiteQuality
SIO_000300: 1.573832e6

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 268

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

African
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allele count: 262
allele frequency: 2.532869296210364e-2
allele num: 10344
num of homozygotes: 5

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

Latino
type: Population
allele count: 10
allele frequency: 8.771929824561404e-4
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.051071039574004e-5
allele num: 66104
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
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SIO_000300: 5.993e1

VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.5e-2

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11386
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: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

African
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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
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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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num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
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African
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allele frequency: 4.868549172346641e-4
allele num: 10270
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521977352976988e-5
allele num: 65704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 2.826e0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

MQ
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SIO_000300: 5.959e1

QD
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SIO_000300: 1.062e1

ReadPosRankSum
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SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: -4.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e0

DP
type: SiteQuality
SIO_000300: 1.537722e6

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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bin: 9.75e1
variant carriers: 51

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 567
bin: 3.75e1
variant carriers: 0

African
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allele count: 49
allele frequency: 4.772107518504091e-3
allele num: 10268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.767408978437611e-4
allele num: 11316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15002
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65670
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.39e1

ReadPosRankSum
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SIO_000300: 1.39e-1

VQSLOD
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MQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

DP
type: SiteQuality
SIO_000300: 1.536047e6

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524390243902439e-5
allele num: 65600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14922
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.197e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 1.525398e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65482
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14874
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.065e0

VQSLOD
type: SiteQuality
SIO_000300: -2.393e0

FS
type: SiteQuality
SIO_000300: 1.524e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.858e1

QD
type: SiteQuality
SIO_000300: 1.254e1

DP
type: SiteQuality
SIO_000300: 1.514558e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
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: 0
allele frequency: 0.0e0
allele num: 65470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.732193348592971e-5
allele num: 14854
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.737e1

VQSLOD
type: SiteQuality
SIO_000300: -3.984e-1

BaseQRankSum
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SIO_000300: 3.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.510063e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 42

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14758
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.526538280883044e-3
allele num: 8516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.654623392529087e-4
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.517572569051479e-4
allele num: 65386
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.697e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.173e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 75

GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.13685179502915e-4
allele num: 6518
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 69
allele frequency: 1.058249746940278e-3
allele num: 65202
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.958096729978461e-4
allele num: 10214
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
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QD
type: SiteQuality
SIO_000300: 1.366e1

DP
type: SiteQuality
SIO_000300: 1.460256e6

MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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ReadPosRankSum
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SIO_000300: 4.01e-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: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543591010125957e-5
allele num: 64784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.424e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 9.56e-1

ClippingRankSum
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SIO_000300: -6.26e-1

VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3993
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24703
bin: 9.75e1
variant carriers: 694

African
type: Population
allele count: 672
allele frequency: 6.509104998062766e-2
allele num: 10324
num of homozygotes: 34

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

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

Latino
type: Population
allele count: 29
allele frequency: 2.517361111111111e-3
allele num: 11520
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.358490566037736e-3
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.513810804204351e-4
allele num: 65456
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.576789656259855e-4
allele num: 12684
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.710000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e0

QD
type: SiteQuality
SIO_000300: 1.486e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.64e0

DP
type: SiteQuality
SIO_000300: 2.674845e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

GenotypeQuality
all individuals: 577
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3900
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.5e0
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GenotypeQuality
all individuals: 24394
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4941
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9784
bin: 6.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528070657987225e-5
allele num: 65442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12684
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.429999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

DP
type: SiteQuality
SIO_000300: 2.65569e6

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 24395
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65484
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12740
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

DP
type: SiteQuality
SIO_000300: 2.65613e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 4950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 570
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variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24395
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.054181174027243e-5
allele num: 65484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

DP
type: SiteQuality
SIO_000300: 2.65613e6

QD
type: SiteQuality
SIO_000300: 1.334e1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9887
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.565435190983093e-4
allele num: 12776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.05446104034943e-5
allele num: 65478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.491620111731844e-4
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 4.343e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

QD
type: SiteQuality
SIO_000300: 1.274e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

DP
type: SiteQuality
SIO_000300: 2.656818e6

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
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: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12988
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

FS
type: SiteQuality
SIO_000300: 2.033e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

DP
type: SiteQuality
SIO_000300: 2.65855e6

QD
type: SiteQuality
SIO_000300: 7.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.069e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
all individuals: 2191
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 636
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4978
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 10464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24562
bin: 9.75e1
variant carriers: 450

GenotypeQuality
all individuals: 2367
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3907
bin: 8.25e1
variant carriers: 10

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.090319437254484e-5
allele num: 65678
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.496503496503497e-3
allele num: 858
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 371
allele frequency: 2.790732661350985e-2
allele num: 13294
num of homozygotes: 7

Latino
type: Population
allele count: 10
allele frequency: 8.673026886383347e-4
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 77
allele frequency: 7.445368400696191e-3
allele num: 10342
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.59e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

QD
type: SiteQuality
SIO_000300: 1.482e1

DP
type: SiteQuality
SIO_000300: 2.668993e6

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24227
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
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GenotypeQuality
all individuals: 10726
bin: 6.25e1
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GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
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GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521745746720638e-5
allele num: 65714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.659448e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

FS
type: SiteQuality
SIO_000300: 3.565e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.654e1

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4043
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24227
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.180812868016659e-5
allele num: 13926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03692905733722e-5
allele num: 65856
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

FS
type: SiteQuality
SIO_000300: 3.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.670099e6

QD
type: SiteQuality
SIO_000300: 1.181e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.76e-1

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11872
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 26
allele frequency: 1.831759898548683e-3
allele num: 14194
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51666818333485e-5
allele num: 65934
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 2.674781e6

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

FS
type: SiteQuality
SIO_000300: 1.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3921
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5125
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24216
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

QD
type: SiteQuality
SIO_000300: 1.177e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.767e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 2.67873e6

GenotypeQuality
all individuals: 2396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4051
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12177
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24215
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 4
allele frequency: 4.63821892393321e-4
allele num: 8624
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.031e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 5.308e0

DP
type: SiteQuality
SIO_000300: 2.680168e6

GenotypeQuality
all individuals: 5144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12380
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24214
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14614
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: -3.125e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.094e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 2.681766e6

FS
type: SiteQuality
SIO_000300: 3.974e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.708e0

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24213
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13197
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variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15268
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 2.694306e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.407e0

QD
type: SiteQuality
SIO_000300: 1.097e1

GenotypeQuality
all individuals: 2075
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13523
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15470
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.513e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e0

DP
type: SiteQuality
SIO_000300: 2.697811e6

VQSLOD
type: SiteQuality
SIO_000300: -7.368e-1

FS
type: SiteQuality
SIO_000300: 1.681e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.187e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.806e0

GenotypeQuality
all individuals: 5351
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24213
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3919
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14534
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.228199459592238e-4
allele num: 16284
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.517e1

VQSLOD
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
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MQRankSum
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DP
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (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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European (Non-Finnish)
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Other
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FS
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DP
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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South Asian
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European (Finnish)
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Latino
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East Asian
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African
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Other
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European (Non-Finnish)
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8590
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African
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European (Finnish)
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South Asian
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Other
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Latino
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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MQ
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DP
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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African
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Other
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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QD
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VQSLOD
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DP
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MQRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Latino
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Other
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Other
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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QD
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MQRankSum
type: SiteQuality
SIO_000300: -1.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

DP
type: SiteQuality
SIO_000300: 2.712779e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.68e-1

GenotypeQuality
all individuals: 14589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24206
bin: 9.75e1
variant carriers: 133

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3916
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2429
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 95
allele frequency: 8.245096337441417e-3
allele num: 11522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.015218502812114e-5
allele num: 66498
num of homozygotes: 0

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

East Asian
type: Population
allele count: 35
allele frequency: 4.088785046728972e-3
allele num: 8560
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

DP
type: SiteQuality
SIO_000300: 2.712854e6

QD
type: SiteQuality
SIO_000300: 1.559e1

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

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

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

GenotypeQuality
all individuals: 2082
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4068
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5291
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.821e0

MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

DP
type: SiteQuality
SIO_000300: 2.707956e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.776e0

QD
type: SiteQuality
SIO_000300: 1.223e1

VQSLOD
type: SiteQuality
SIO_000300: -4.189e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0