6-166902271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902271
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902271
    reference: chr 6
allele count: 1
allele frequency: 1.101952660113722e-5
allele num: 90748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+50C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19423
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5165
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8358
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

6-166902273-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902273
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902273
    reference: chr 6
allele count: 1
allele frequency: 1.092585713349212e-5
allele num: 91526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+48C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+48C>G
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11483
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9024
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-166902273-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902273
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902273
    reference: chr 6
allele count: 1
allele frequency: 1.092585713349212e-5
allele num: 91526
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+48C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+48C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

6-166902279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902279
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902279
    reference: chr 6
allele count: 13
allele frequency: 1.411938482926405e-4
allele num: 92072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+42C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+42C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19078
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7969
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12629
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6647
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5065
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

6-166902279-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902279
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902279
    reference: chr 6
allele count: 2
allele frequency: 2.172213050656008e-5
allele num: 92072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+42C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+42C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19078
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6647
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7969
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-166902281-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902281
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902282
    reference: chr 6
allele count: 1
allele frequency: 1.07914445427665e-5
allele num: 92666
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+39_445+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+39_982+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+39_640+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+39_640+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+39_562+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+39_931+40insT
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+39_907+40insT
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12934
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4991
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-166902282-C-CGGTAGCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902282
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902289
    reference: chr 6
allele count: 1
allele frequency: 1.077655882923465e-5
allele num: 92794
alternate allele: CGGTAGCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+38_640+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+38_931+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+38_982+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+38_562+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+38_640+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+38_445+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+38_907+39insAGCTACC
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4959
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

6-166902286-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902286
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902286
    reference: chr 6
allele count: 1
allele frequency: 1.067418129029504e-5
allele num: 93684
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+35T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+35T>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5067
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

6-166902287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902287
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902287
    reference: chr 6
allele count: 1
allele frequency: 1.068490223314457e-5
allele num: 93590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+34G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16281
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4652
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

6-166902292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902292
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902292
    reference: chr 6
allele count: 3
allele frequency: 3.150201612903226e-5
allele num: 95232
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+29G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+29G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20872
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

6-166911948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911948
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911948
    reference: chr 6
allele count: 1
allele frequency: 9.853575862680566e-6
allele num: 101486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+48G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14864
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

6-166902293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902293
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902293
    reference: chr 6
allele count: 1
allele frequency: 1.046966936784136e-5
allele num: 95514
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+28G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+28G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21594
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3980
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3309
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24754
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-166902297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902297
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902297
    reference: chr 6
allele count: 2
allele frequency: 2.044947956074518e-5
allele num: 97802
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+24C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+24C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2439
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

6-166902302-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902302
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902302
    reference: chr 6
allele count: 2
allele frequency: 2.009444388626545e-5
allele num: 99530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+19C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+19C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-166902306-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902306
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902306
    reference: chr 6
allele count: 1
allele frequency: 9.850663934749202e-6
allele num: 101516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+15G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+15G>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3033
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

6-166902309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902309
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902309
    reference: chr 6
allele count: 71
allele frequency: 6.864678810380168e-4
allele num: 103428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+12C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 30604
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9307
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-166902319-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902319
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902319
    reference: chr 6
allele count: 10
allele frequency: 9.366453111535724e-5
allele num: 106764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.445+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.640+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.907+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.640+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.982+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.562+2T>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.931+2T>G
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33212
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7233
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
hgvs: c.931+2T>G
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/6-166902325-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902325
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902325
    reference: chr 6
allele count: 4
allele frequency: 3.63550433533892e-5
allele num: 110026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.636G>T
  hgvsp: ENST00000405189.3:c.636G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.978G>T
  hgvsp: ENST00000510118.1:c.978G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.927G>T
  hgvsp: ENST00000503859.1:c.927G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.558G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.903G>T
  hgvsp: ENST00000265678.4:c.903G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.636G>T
  hgvsp: ENST00000481261.2:c.636G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.441G>T
  hgvsp: ENST00000366863.2:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34951
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg309Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/6-166902326-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902326
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902326
    reference: chr 6
allele count: 1
allele frequency: 9.040120052794301e-6
allele num: 110618
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.926G>T
  hgvsp: ENSP00000427015.1:p.Arg309Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.440G>T
  hgvsp: ENSP00000355828.2:p.Arg147Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.635G>T
  hgvsp: ENSP00000422484.1:p.Arg212Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.557G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.977G>T
  hgvsp: ENSP00000422435.1:p.Arg326Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.635G>T
  hgvsp: ENSP00000386050.3:p.Arg212Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.902G>T
  hgvsp: ENSP00000265678.4:p.Arg301Leu
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11727
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg309Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-166902346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902346
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902346
    reference: chr 6
allele count: 1
allele frequency: 8.725242125468982e-6
allele num: 114610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.537C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.957C>T
  hgvsp: ENST00000510118.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.615C>T
  hgvsp: ENST00000481261.2:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.420C>T
  hgvsp: ENST00000366863.2:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.615C>T
  hgvsp: ENST00000405189.3:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.906C>T
  hgvsp: ENST00000503859.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.882C>T
  hgvsp: ENST00000265678.4:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47029
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe302Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

6-166902351-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902351
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902351
    reference: chr 6
allele count: 1
allele frequency: 8.709739230407442e-6
allele num: 114814
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.610C>G
  hgvsp: ENSP00000386050.3:p.Leu204Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.415C>G
  hgvsp: ENSP00000355828.2:p.Leu139Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.877C>G
  hgvsp: ENSP00000265678.4:p.Leu293Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.532C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.952C>G
  hgvsp: ENSP00000422435.1:p.Leu318Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.901C>G
  hgvsp: ENSP00000427015.1:p.Leu301Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.610C>G
  hgvsp: ENSP00000422484.1:p.Leu204Val
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu301Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

6-166902356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902356
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902356
    reference: chr 6
allele count: 2
allele frequency: 1.740068558701213e-5
allele num: 114938
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.896G>A
  hgvsp: ENSP00000427015.1:p.Arg299Gln
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.605G>A
  hgvsp: ENSP00000386050.3:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.872G>A
  hgvsp: ENSP00000265678.4:p.Arg291Gln
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.947G>A
  hgvsp: ENSP00000422435.1:p.Arg316Gln
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.410G>A
  hgvsp: ENSP00000355828.2:p.Arg137Gln
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.527G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.605G>A
  hgvsp: ENSP00000422484.1:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg299Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/6-166902376-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902376
    reference: chr 6
allele count: 18
allele frequency: 1.577563540753725e-4
allele num: 114100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.585G>T
  hgvsp: ENST00000405189.3:c.585G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.876G>T
  hgvsp: ENST00000503859.1:c.876G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.927G>T
  hgvsp: ENST00000510118.1:c.927G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.585G>T
  hgvsp: ENST00000481261.2:c.585G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.507G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.852G>T
  hgvsp: ENST00000265678.4:c.852G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.390G>T
  hgvsp: ENST00000366863.2:c.390G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35716
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14120
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5051
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly292Gly
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

6-166902377-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902377
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902377
    reference: chr 6
allele count: 89
allele frequency: 7.806606669824395e-4
allele num: 114006
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.875G>C
  hgvsp: ENSP00000427015.1:p.Gly292Ala
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.389G>C
  hgvsp: ENSP00000355828.2:p.Gly130Ala
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.851G>C
  hgvsp: ENSP00000265678.4:p.Gly284Ala
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.584G>C
  hgvsp: ENSP00000386050.3:p.Gly195Ala
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.584G>C
  hgvsp: ENSP00000422484.1:p.Gly195Ala
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.506G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.926G>C
  hgvsp: ENSP00000422435.1:p.Gly309Ala
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14191
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 35483
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 9.75e1
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly292Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-166902388-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902388
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902388
    reference: chr 6
allele count: 1
allele frequency: 8.912338241060925e-6
allele num: 112204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.573G>C
  hgvsp: ENSP00000386050.3:p.Gln191His
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.864G>C
  hgvsp: ENSP00000427015.1:p.Gln288His
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.573G>C
  hgvsp: ENSP00000422484.1:p.Gln191His
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.495G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.840G>C
  hgvsp: ENSP00000265678.4:p.Gln280His
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.915G>C
  hgvsp: ENSP00000422435.1:p.Gln305His
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.378G>C
  hgvsp: ENSP00000355828.2:p.Gln126His
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43958
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln288His
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

6-166902392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902392
    reference: chr 6
allele count: 1
allele frequency: 9.037178954217652e-6
allele num: 110654
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.860C>T
  hgvsp: ENSP00000427015.1:p.Pro287Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.836C>T
  hgvsp: ENSP00000265678.4:p.Pro279Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.491C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.374C>T
  hgvsp: ENSP00000355828.2:p.Pro125Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.911C>T
  hgvsp: ENSP00000422435.1:p.Pro304Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.569C>T
  hgvsp: ENSP00000386050.3:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.569C>T
  hgvsp: ENSP00000422484.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8725
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro287Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

6-166902406-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902406
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902406
    reference: chr 6
allele count: 1
allele frequency: 9.62334237927517e-6
allele num: 103914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.360C>G
  hgvsp: ENST00000366863.2:c.360C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.897C>G
  hgvsp: ENST00000510118.1:c.897C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.822C>G
  hgvsp: ENST00000265678.4:c.822C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.555C>G
  hgvsp: ENST00000405189.3:c.555C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.477C>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.846C>G
  hgvsp: ENST00000503859.1:c.846C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.555C>G
  hgvsp: ENST00000481261.2:c.555C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala282Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

6-166902419-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902419
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902419
    reference: chr 6
allele count: 1
allele frequency: 1.054607580519289e-5
allele num: 94822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.357-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.552-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.894-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.843-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.474-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.552-10T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.819-10T>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26533
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2706
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

6-166902431-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902431
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902431
    reference: chr 6
allele count: 104
allele frequency: 1.229750502542273e-3
allele num: 84570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.552-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.552-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.819-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.894-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.357-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.843-22A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.474-22A>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 24790
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3567
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31294
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-166902432-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902432
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902432
    reference: chr 6
allele count: 1
allele frequency: 1.184693756663902e-5
allele num: 84410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.894-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.843-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.552-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.819-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.474-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.552-23T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.357-23T>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9843
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31541
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

6-166902434-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902434
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902434
    reference: chr 6
allele count: 1
allele frequency: 1.214919207872676e-5
allele num: 82310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.894-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.474-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.357-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.552-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.819-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.552-25C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.843-25C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3853
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

6-166902457-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166902457
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166902457
    reference: chr 6
allele count: 1
allele frequency: 1.770162146852652e-5
allele num: 56492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.819-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.552-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.894-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.843-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.357-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.474-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.552-48G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9071
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7704
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-166904121-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904121
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904121
    reference: chr 6
allele count: 2
allele frequency: 3.514567883878677e-5
allele num: 56906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.893+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.818+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.473+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.356+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.551+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.551+38A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.842+38A>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14732
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4861
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5862
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4861
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

6-166904125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904125
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904125
    reference: chr 6
allele count: 2
allele frequency: 3.427827100401056e-5
allele num: 58346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.551+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.893+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.551+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.473+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.842+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.818+34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.356+34G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14649
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2139
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23529
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5070
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

6-166904126-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904126
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904126
    reference: chr 6
allele count: 6
allele frequency: 1.02124183006536e-4
allele num: 58752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.842+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.473+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.551+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.818+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.356+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.551+33C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.893+33C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26211
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14466
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

6-166904142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904142
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904142
    reference: chr 6
allele count: 1
allele frequency: 1.497588881900141e-5
allele num: 66774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.473+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.818+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.893+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.356+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.842+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.551+17C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.551+17C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11454
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-166904163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904163
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904163
    reference: chr 6
allele count: 1
allele frequency: 1.225400093130407e-5
allele num: 81606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.814C>T
  hgvsp: ENSP00000265678.4:p.Leu272Phe
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.838C>T
  hgvsp: ENSP00000427015.1:p.Leu280Phe
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.469C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.889C>T
  hgvsp: ENSP00000422435.1:p.Leu297Phe
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.547C>T
  hgvsp: ENSP00000422484.1:p.Leu183Phe
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.352C>T
  hgvsp: ENSP00000355828.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.547C>T
  hgvsp: ENSP00000386050.3:p.Leu183Phe
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20204
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2424
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu280Phe
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-166904167-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904167
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904167
    reference: chr 6
allele count: 3
allele frequency: 3.56641860243943e-5
allele num: 84118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.810C>T
  hgvsp: ENST00000265678.4:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.885C>T
  hgvsp: ENST00000510118.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.543C>T
  hgvsp: ENST00000481261.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.543C>T
  hgvsp: ENST00000405189.3:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.348C>T
  hgvsp: ENST00000366863.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.834C>T
  hgvsp: ENST00000503859.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.465C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21557
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22421
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu278Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-166904182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904182
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904182
    reference: chr 6
allele count: 1
allele frequency: 1.070778455937467e-5
allele num: 93390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.450G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.528G>A
  hgvsp: ENST00000405189.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.819G>A
  hgvsp: ENST00000503859.1:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.795G>A
  hgvsp: ENST00000265678.4:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.333G>A
  hgvsp: ENST00000366863.2:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.528G>A
  hgvsp: ENST00000481261.2:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.870G>A
  hgvsp: ENST00000510118.1:c.870G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys273Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-166904194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904194
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904194
    reference: chr 6
allele count: 1
allele frequency: 1.016033000751864e-5
allele num: 98422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.516G>A
  hgvsp: ENST00000405189.3:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.321G>A
  hgvsp: ENST00000366863.2:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.858G>A
  hgvsp: ENST00000510118.1:c.858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.516G>A
  hgvsp: ENST00000481261.2:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.807G>A
  hgvsp: ENST00000503859.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.438G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.783G>A
  hgvsp: ENST00000265678.4:c.783G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13102
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly269Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-166904196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904196
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904196
    reference: chr 6
allele count: 1
allele frequency: 1.012986486760267e-5
allele num: 98718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.514G>A
  hgvsp: ENSP00000422484.1:p.Gly172Arg
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.781G>A
  hgvsp: ENSP00000265678.4:p.Gly261Arg
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.856G>A
  hgvsp: ENSP00000422435.1:p.Gly286Arg
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.436G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.805G>A
  hgvsp: ENSP00000427015.1:p.Gly269Arg
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.514G>A
  hgvsp: ENSP00000386050.3:p.Gly172Arg
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.319G>A
  hgvsp: ENSP00000355828.2:p.Gly107Arg
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13051
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30620
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly269Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

6-166904203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904203
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904203
    reference: chr 6
allele count: 10
allele frequency: 1.002044170107018e-4
allele num: 99796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.507G>A
  hgvsp: ENST00000405189.3:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.312G>A
  hgvsp: ENST00000366863.2:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.798G>A
  hgvsp: ENST00000503859.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.774G>A
  hgvsp: ENST00000265678.4:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.849G>A
  hgvsp: ENST00000510118.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.507G>A
  hgvsp: ENST00000481261.2:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.429G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27999
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro266Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

6-166904212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904212
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904212
    reference: chr 6
allele count: 1749
allele frequency: 1.737290660945229e-2
allele num: 100674
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.789G>A
  hgvsp: ENST00000503859.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.498G>A
  hgvsp: ENST00000481261.2:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.303G>A
  hgvsp: ENST00000366863.2:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.498G>A
  hgvsp: ENST00000405189.3:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.765G>A
  hgvsp: ENST00000265678.4:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.840G>A
  hgvsp: ENST00000510118.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.420G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26776
  bin: 2.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 7.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 6985
  bin: 2.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 1.75e1
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 1.25e1
  variant carriers: 236
genotype quality: GenotypeQuality
  all individuals: 12906
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 6.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 29323
  bin: 6.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 7.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.75e1
  variant carriers: 10
hgvs: p.Gly263Gly
num of homozygotes: 16
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-166904215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904215
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904215
    reference: chr 6
allele count: 4
allele frequency: 3.992892651081076e-5
allele num: 100178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.495G>A
  hgvsp: ENST00000405189.3:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.837G>A
  hgvsp: ENST00000510118.1:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.300G>A
  hgvsp: ENST00000366863.2:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.786G>A
  hgvsp: ENST00000503859.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.495G>A
  hgvsp: ENST00000481261.2:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.762G>A
  hgvsp: ENST00000265678.4:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.417G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26617
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7049
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29981
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Thr262Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

6-166904216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904216
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904216
    reference: chr 6
allele count: 4
allele frequency: 3.993291270665283e-5
allele num: 100168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.761C>T
  hgvsp: ENSP00000265678.4:p.Thr254Met
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.416C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.494C>T
  hgvsp: ENSP00000386050.3:p.Thr165Met
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.494C>T
  hgvsp: ENSP00000422484.1:p.Thr165Met
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.836C>T
  hgvsp: ENSP00000422435.1:p.Thr279Met
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.299C>T
  hgvsp: ENSP00000355828.2:p.Thr100Met
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.785C>T
  hgvsp: ENSP00000427015.1:p.Thr262Met
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26539
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29943
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13777
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr262Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-166904218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904218
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904218
    reference: chr 6
allele count: 946
allele frequency: 9.422498456144545e-3
allele num: 100398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.492C>T
  hgvsp: ENST00000405189.3:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.834C>T
  hgvsp: ENST00000510118.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.759C>T
  hgvsp: ENST00000265678.4:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.414C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.297C>T
  hgvsp: ENST00000366863.2:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.783C>T
  hgvsp: ENST00000503859.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.492C>T
  hgvsp: ENST00000481261.2:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 1.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 1.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 7.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 26032
  bin: 2.25e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 3.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 2.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13893
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 8.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Leu261Leu
num of homozygotes: 40
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

6-166904222-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904222
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904222
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 100008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.755T>A
  hgvsp: ENSP00000265678.4:p.Met252Lys
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.410T>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.779T>A
  hgvsp: ENSP00000427015.1:p.Met260Lys
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.293T>A
  hgvsp: ENSP00000355828.2:p.Met98Lys
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.830T>A
  hgvsp: ENSP00000422435.1:p.Met277Lys
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.488T>A
  hgvsp: ENSP00000422484.1:p.Met163Lys
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.488T>A
  hgvsp: ENSP00000386050.3:p.Met163Lys
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14810
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met260Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

6-166904247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904247
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904247
    reference: chr 6
allele count: 1
allele frequency: 1.030311772342311e-5
allele num: 97058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-18C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-166904248-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904248
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904248
    reference: chr 6
allele count: 1
allele frequency: 1.032119560729915e-5
allele num: 96888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-19G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-19G>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15690
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3960
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/6-166904259-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904259
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904259
    reference: chr 6
allele count: 2
allele frequency: 2.107836937734497e-5
allele num: 94884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-30G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-30G>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6315
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21057
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

6-166904259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904259
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904259
    reference: chr 6
allele count: 1
allele frequency: 1.053918468867248e-5
allele num: 94884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-30G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-30G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20299
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 674
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 6315
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 571
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

6-166904263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904263
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904263
    reference: chr 6
allele count: 4
allele frequency: 4.256043581886278e-5
allele num: 93984
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-34G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-34G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

6-166904265-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904265
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904265
    reference: chr 6
allele count: 1
allele frequency: 1.067896883876893e-5
allele num: 93642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-36A>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-36A>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum

6-166904277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904277
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904277
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 84640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-48G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-48G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15165
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-166904278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904278
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904278
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 84812
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-49C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-49C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7809
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

6-166904279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166904279
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166904279
    reference: chr 6
allele count: 1
allele frequency: 1.177163037080636e-5
allele num: 84950
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.772-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.481-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.286-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.823-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.481-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.748-50C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.403-50C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5262
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

6-166911948-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911948
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911948
    reference: chr 6
allele count: 1
allele frequency: 9.853575862680566e-6
allele num: 101486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+48G>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+48G>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-166911949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911949
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911949
    reference: chr 6
allele count: 20
allele frequency: 1.96382631920033e-4
allele num: 101842
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+47C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+47C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13734
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8367
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17769
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11545
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8720
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/6-166911961-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911961
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 103286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+35G>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+35G>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-166911961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911961
    reference: chr 6
allele count: 8
allele frequency: 7.745483414983638e-5
allele num: 103286
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+35G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+35G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6702
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

6-166911962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911962
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911962
    reference: chr 6
allele count: 4
allele frequency: 3.860780263691292e-5
allele num: 103606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+34C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+34C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19406
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15462
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-166911966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911966
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911966
    reference: chr 6
allele count: 1
allele frequency: 9.535251826000725e-6
allele num: 104874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+30A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+30A>G
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-166911968-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911968
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911968
    reference: chr 6
allele count: 1
allele frequency: 9.52580540684715e-6
allele num: 104978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+28C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+28C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20994
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8844
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3842
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-166911970-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911970
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911970
    reference: chr 6
allele count: 1
allele frequency: 9.450545296463605e-6
allele num: 105814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+26T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+26T>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3671
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8649
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-166911975-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911975
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911975
    reference: chr 6
allele count: 2
allele frequency: 1.871327519742505e-5
allele num: 106876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+21T>C
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+21T>C
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

6-166911978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911978
    reference: chr 6
allele count: 1
allele frequency: 9.304749143963078e-6
allele num: 107472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+18C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+18C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7905
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

6-166911982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911982
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911982
    reference: chr 6
allele count: 2
allele frequency: 1.851817558934094e-5
allele num: 108002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+14G>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+14G>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24198
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3013
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-166911983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911983
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911983
    reference: chr 6
allele count: 1
allele frequency: 9.180376028202115e-6
allele num: 108928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+13C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+13C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2773
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

6-166911984-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911984
    reference: chr 6
allele count: 1
allele frequency: 9.130418903619297e-6
allele num: 109524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+12C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+12C>T
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-166911990-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911990
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911990
    reference: chr 6
allele count: 1
allele frequency: 8.953353030710001e-6
allele num: 111690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.402+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.285+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.771+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.480+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.822+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.480+6C>A
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.747+6C>A
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
hgvs: c.771+6C>A
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

6-166911998-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911998
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911998
    reference: chr 6
allele count: 2
allele frequency: 1.751835047211954e-5
allele num: 114166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.283A>G
  hgvsp: ENSP00000355828.2:p.Met95Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.400A>G
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.820A>G
  hgvsp: ENSP00000422435.1:p.Met274Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.478A>G
  hgvsp: ENSP00000422484.1:p.Met160Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.478A>G
  hgvsp: ENSP00000386050.3:p.Met160Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.745A>G
  hgvsp: ENSP00000265678.4:p.Met249Val
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.769A>G
  hgvsp: ENSP00000427015.1:p.Met257Val
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32318
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30883
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met257Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

6-166911999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 166911999
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 166911999
    reference: chr 6
allele count: 1
allele frequency: 8.746457684637721e-6
allele num: 114332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071242
  ensembl transcript: ENST00000366865
  gene symbol: RPS6KA2
  hgvsc: ENST00000366865.1:n.399C>T
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000427015
  ensembl transcript: ENST00000503859
  gene symbol: RPS6KA2
  hgvsc: ENST00000503859.1:c.768C>T
  hgvsp: ENST00000503859.1:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000355828
  ensembl transcript: ENST00000366863
  gene symbol: RPS6KA2
  hgvsc: ENST00000366863.2:c.282C>T
  hgvsp: ENST00000366863.2:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000386050
  ensembl transcript: ENST00000405189
  gene symbol: RPS6KA2
  hgvsc: ENST00000405189.3:c.477C>T
  hgvsp: ENST00000405189.3:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422435
  ensembl transcript: ENST00000510118
  gene symbol: RPS6KA2
  hgvsc: ENST00000510118.1:c.819C>T
  hgvsp: ENST00000510118.1:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000422484
  ensembl transcript: ENST00000481261
  gene symbol: RPS6KA2
  hgvsc: ENST00000481261.2:c.477C>T
  hgvsp: ENST00000481261.2:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071242
  ensembl protein: ENSP00000265678
  ensembl transcript: ENST00000265678
  gene symbol: RPS6KA2
  hgvsc: ENST00000265678.4:c.744C>T
  hgvsp: ENST00000265678.4:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10431
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu256Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 532
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2612
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6941
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11155
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.03715775749674e-5
allele num: 49088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

DP
type: SiteQuality
SIO_000300: 9.33081e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.477e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13580
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.311647429171039e-4
allele num: 7624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6802
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.35426e5

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49518
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.470155836518671e-4
allele num: 6802
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

DP
type: SiteQuality
SIO_000300: 9.35426e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

QD
type: SiteQuality
SIO_000300: 4.74e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 5.538e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 2.268602540834846e-4
allele num: 8816
num of homozygotes: 0

European (Non-Finnish)
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allele count: 11
allele frequency: 2.207062600321027e-4
allele num: 49840
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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.8e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 9.61104e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.456876456876457e-4
allele num: 6864
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.306165099268548e-4
allele num: 7656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49840
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 9.61104e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

FS
type: SiteQuality
SIO_000300: 8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-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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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.444669170759896e-4
allele num: 6922
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4638
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.151e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

DP
type: SiteQuality
SIO_000300: 9.7622e5

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

QD
type: SiteQuality
SIO_000300: 7.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.371e0

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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50260
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13658
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East Asian
type: Population
allele count: 1
allele frequency: 1.445504481063891e-4
allele num: 6918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7712
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.183e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.84019e5

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

South Asian
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allele frequency: 7.279079924297569e-5
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num of homozygotes: 0

East Asian
type: Population
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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: 50758
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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allele num: 690
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African
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BaseQRankSum
type: SiteQuality
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DP
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.782999999999999e0

VQSLOD
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.972620033929065e-5
allele num: 50694
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4712
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 5.802932415180471e-5
allele num: 51698
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

Other
type: Population
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.059308072487644e-4
allele num: 4856
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 4.824e0

DP
type: SiteQuality
SIO_000300: 1.036176e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.276e1

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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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.927599367747408e-5
allele num: 51878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -1.147e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 1.084621e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.457e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53362
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.158196134574088e-5
allele num: 13970
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.350621285791464e-4
allele num: 7404
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.129271e6

QD
type: SiteQuality
SIO_000300: 9.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

FS
type: SiteQuality
SIO_000300: 1.427e0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.673499375505106e-5
allele num: 54444
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14092
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.161991e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 1.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.796880615251923e-5
allele num: 55652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

QD
type: SiteQuality
SIO_000300: 1.169e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.3e-1

FS
type: SiteQuality
SIO_000300: 1.494e0

DP
type: SiteQuality
SIO_000300: 1.195984e6

GenotypeQuality
all individuals: 2218
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 71

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.407954945441746e-4
allele num: 56820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5226
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.006018054162487e-4
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7868
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.188212927756654e-4
allele num: 8416
num of homozygotes: 0

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

South Asian
type: Population
allele count: 60
allele frequency: 4.173042147725692e-3
allele num: 14378
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 1.23262e6

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-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
all individuals: 769
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.86706497386109e-4
allele num: 5356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.185275491889329e-4
allele num: 59058
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.339728591483388e-4
allele num: 8548
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

FS
type: SiteQuality
SIO_000300: 2.90151e2

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 1.291037e6

VQSLOD
type: SiteQuality
SIO_000300: -3.864e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.404e0

QD
type: SiteQuality
SIO_000300: 1.2e-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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.496676163342829e-5
allele num: 10530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.924006171421068e-5
allele num: 60926
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.325391e6

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.17e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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African
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5808
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.631268147858145e-5
allele num: 61302
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

DP
type: SiteQuality
SIO_000300: 1.331627e6

FS
type: SiteQuality
SIO_000300: 8.702e0

QD
type: SiteQuality
SIO_000300: 5.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15320
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63614
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African
type: Population
allele count: 1
allele frequency: 1.06473594548552e-4
allele num: 9392
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East Asian
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
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European (Finnish)
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allele count: 0
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allele num: 6116
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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DP
type: SiteQuality
SIO_000300: 1.38768e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47030
bin: 6.25e1
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GenotypeQuality
all individuals: 715
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570302440249992e-5
allele num: 63682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

FS
type: SiteQuality
SIO_000300: 1.377e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 1.037e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.390761e6

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

GenotypeQuality
all individuals: 278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
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GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.138436430970091e-5
allele num: 63726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.887e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.091e0

QD
type: SiteQuality
SIO_000300: 1.447e1

DP
type: SiteQuality
SIO_000300: 1.393981e6

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

GenotypeQuality
all individuals: 730
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 391
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46186
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.852253280091272e-4
allele num: 63108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.572e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.773e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 9.02e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.384465e6

GenotypeQuality
all individuals: 272
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3663
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 46067
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variant carriers: 1

GenotypeQuality
all individuals: 834
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 864
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
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variant carriers: 1

GenotypeQuality
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
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variant carriers: 1

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.221689413500554e-5
allele num: 10844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 67
allele frequency: 1.062884700805889e-3
allele num: 63036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 2.136752136752137e-3
allele num: 6084
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.234916895694281e-4
allele num: 15282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

FS
type: SiteQuality
SIO_000300: 1.161e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.383698e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 9.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeQuality
all individuals: 491
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10670
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615822130299897e-5
allele num: 61888
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 8.832000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

QD
type: SiteQuality
SIO_000300: 1.161e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.35436e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

GenotypeQuality
all individuals: 42302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 512
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GenotypeQuality
all individuals: 221
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variant carriers: 0

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
all individuals: 775
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variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14960
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.641227638273429e-5
allele num: 60930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.334009e6

GenotypeQuality
all individuals: 322
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
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GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
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GenotypeQuality
all individuals: 420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5378
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.928086462519052e-5
allele num: 14434
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.19e0

DP
type: SiteQuality
SIO_000300: 1.21783e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.289e0

VQSLOD
type: SiteQuality
SIO_000300: -1.829e0

FS
type: SiteQuality
SIO_000300: 4.009e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.828e1

GenotypeQuality
all individuals: 614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
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variant carriers: 1

GenotypeQuality
all individuals: 796
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
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GenotypeQuality
all individuals: 248
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.259001161440186e-5
allele num: 13776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 1.309e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

DP
type: SiteQuality
SIO_000300: 1.042369e6

FS
type: SiteQuality
SIO_000300: 1.349e0

MQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

MQ
type: SiteQuality
SIO_000300: 5.884e1

VQSLOD
type: SiteQuality
SIO_000300: -2.856e-1

GenotypeQuality
all individuals: 4143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 9.75e1
variant carriers: 95

GenotypeQuality
all individuals: 303
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 249
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 586
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 1

Latino
type: Population
allele count: 9
allele frequency: 1.184522242695446e-3
allele num: 7598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4336
num of homozygotes: 0

African
type: Population
allele count: 92
allele frequency: 1.223404255319149e-2
allele num: 7520
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.429482636428065e-5
allele num: 45152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.552795031055901e-3
allele num: 644
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

FS
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

QD
type: SiteQuality
SIO_000300: 1.333e1

DP
type: SiteQuality
SIO_000300: 8.67716e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 7.25e1
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GenotypeQuality
all individuals: 218
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
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GenotypeQuality
all individuals: 110
bin: 5.75e1
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GenotypeQuality
all individuals: 785
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.741136398823347e-5
allele num: 12918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.66022e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.805e1

VQSLOD
type: SiteQuality
SIO_000300: -2.297e0

MQRankSum
type: SiteQuality
SIO_000300: -1.259e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.383e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
all individuals: 8470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.829627309740057e-5
allele num: 12772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.798e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.893e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 8.42964e5

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5961
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
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variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.338634237605239e-4
allele num: 4276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.564e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 2.058e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

DP
type: SiteQuality
SIO_000300: 7.01134e5

GenotypeQuality
all individuals: 3158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 518
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.407381303261357e-5
allele num: 31214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.24366e5

QD
type: SiteQuality
SIO_000300: 1.155e1

GenotypeQuality
all individuals: 4244
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5903
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4942
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5382
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.913752913752914e-4
allele num: 3432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.12343828085957e-5
allele num: 32016
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.654e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

DP
type: SiteQuality
SIO_000300: 8.4161e5

FS
type: SiteQuality
SIO_000300: 7.902e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

QD
type: SiteQuality
SIO_000300: 8.34e0

GenotypeQuality
all individuals: 5070
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2869
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.684598378776713e-4
allele num: 5428
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.277904328018223e-4
allele num: 4390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 9.317348903658613e-5
allele num: 32198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

DP
type: SiteQuality
SIO_000300: 8.50066e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 25629
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
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GenotypeQuality
all individuals: 899
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variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 1799
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variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.705042198658299e-5
allele num: 36968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.051e1

DP
type: SiteQuality
SIO_000300: 9.50416e5

MQRankSum
type: SiteQuality
SIO_000300: -1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.64e-1

GenotypeQuality
all individuals: 2811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 741
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20280
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variant carriers: 0

GenotypeQuality
all individuals: 2205
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variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.19751241594515e-5
allele num: 45506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.367e0

DP
type: SiteQuality
SIO_000300: 1.102963e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 4.227733934611048e-4
allele num: 7096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.89e-1

MQ
type: SiteQuality
SIO_000300: 5.816e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.393e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.442e0

DP
type: SiteQuality
SIO_000300: 1.126983e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

QD
type: SiteQuality
SIO_000300: 1.377e1

GenotypeQuality
all individuals: 1031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2671
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 2424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.926188458278758e-5
allele num: 51916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.221254e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

QD
type: SiteQuality
SIO_000300: 1.193e1

FS
type: SiteQuality
SIO_000300: 8.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31006
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.83304615610221e-5
allele num: 54554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.892e0

DP
type: SiteQuality
SIO_000300: 1.271462e6

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.816e1

QD
type: SiteQuality
SIO_000300: 1.339e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.283e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 205
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 920
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1085
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 783
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.827886232360898e-5
allele num: 54708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4788
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.475e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.034e0

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 3.658e0

DP
type: SiteQuality
SIO_000300: 1.273641e6

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 464
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2847
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30877
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.866180048661801e-4
allele num: 8220
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.952029520295203e-4
allele num: 13550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.617421501953408e-5
allele num: 55288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.280335e6

QD
type: SiteQuality
SIO_000300: 1.213e1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 1633
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3872
bin: 9.75e1
variant carriers: 1602

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 852
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1124
bin: 5.25e1
variant carriers: 9

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 140
allele frequency: 2.831715210355987e-2
allele num: 4944
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.515151515151515e-2
allele num: 726
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 2.90065264684554e-3
allele num: 8274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1414
allele frequency: 2.530150663851412e-2
allele num: 55886
num of homozygotes: 14

Latino
type: Population
allele count: 78
allele frequency: 8.021390374331552e-3
allele num: 9724
num of homozygotes: 1

South Asian
type: Population
allele count: 82
allele frequency: 6.00908691191558e-3
allele num: 13646
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 1.282532e6

FS
type: SiteQuality
SIO_000300: 1.817e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
all individuals: 2946
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 2
allele frequency: 2.413127413127413e-4
allele num: 8288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.803426510369702e-5
allele num: 55450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.342281879194631e-4
allele num: 7450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.2673e1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.301e0

DP
type: SiteQuality
SIO_000300: 1.263375e6

GenotypeQuality
all individuals: 468
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 921
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2326
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.93513354857646e-4
allele num: 13628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.26106e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.88e0

QD
type: SiteQuality
SIO_000300: 9.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e-1

GenotypeQuality
all individuals: 1961
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 640
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1074
bin: 7.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2941
bin: 6.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 476
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 29481
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 527
bin: 9.25e1
variant carriers: 14

GenotypeQuality
all individuals: 885
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 3019
bin: 9.75e1
variant carriers: 831

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.248042152369266e-4
allele num: 55418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

Latino
type: Population
allele count: 39
allele frequency: 4.018133113538018e-3
allele num: 9706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7442
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 5.54016620498615e-3
allele num: 722
num of homozygotes: 0

African
type: Population
allele count: 879
allele frequency: 1.029997656433091e-1
allele num: 8534
num of homozygotes: 40

South Asian
type: Population
allele count: 6
allele frequency: 4.393673110720562e-4
allele num: 13656
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.26504e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.602e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.71e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

GenotypeQuality
all individuals: 598
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28581
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.386e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 1.243303e6

FS
type: SiteQuality
SIO_000300: 9.699999999999999e0

QD
type: SiteQuality
SIO_000300: 4.94e0

GenotypeQuality
all individuals: 392
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7092
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.243781094527363e-4
allele num: 8040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13460
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.718e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

QD
type: SiteQuality
SIO_000300: 3.3e0

VQSLOD
type: SiteQuality
SIO_000300: -1.259e0

FS
type: SiteQuality
SIO_000300: 1.711e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.136425e6

GenotypeQuality
all individuals: 2085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 358
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19942
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075268817204301e-4
allele num: 9300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13462
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 9.94e0

DP
type: SiteQuality
SIO_000300: 1.129315e6

GenotypeQuality
all individuals: 658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12793
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.197802197802198e-4
allele num: 9100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13280
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
SIO_000300: 1.724e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

DP
type: SiteQuality
SIO_000300: 1.053051e6

GenotypeQuality
all individuals: 652
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.456452082726478e-4
allele num: 6866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.053051e6

MQ
type: SiteQuality
SIO_000300: 5.895e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.366e0

FS
type: SiteQuality
SIO_000300: 1.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2243
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 881
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.570694087403599e-4
allele num: 7780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.1101243339254e-4
allele num: 9008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13180
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.470588235294118e-3
allele num: 680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

DP
type: SiteQuality
SIO_000300: 1.027361e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.162e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.092e1

FS
type: SiteQuality
SIO_000300: 3.351e0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
all individuals: 9083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 639
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variant carriers: 0

GenotypeQuality
all individuals: 5639
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.928491533922166e-5
allele num: 51854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.111e0

QD
type: SiteQuality
SIO_000300: 1.242e1

VQSLOD
type: SiteQuality
SIO_000300: -1.376e0

FS
type: SiteQuality
SIO_000300: 3.214e0

DP
type: SiteQuality
SIO_000300: 1.014888e6

MQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

GenotypeQuality
all individuals: 2828
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5529
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variant carriers: 0

GenotypeQuality
all individuals: 2655
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 790
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variant carriers: 1

GenotypeQuality
all individuals: 771
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.62986e5

QD
type: SiteQuality
SIO_000300: 1.475e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.203e0

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

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5325
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variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 3.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.714e0

DP
type: SiteQuality
SIO_000300: 9.61921e5

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1127
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.259445843828715e-4
allele num: 7940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5830
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.61227e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.378e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

QD
type: SiteQuality
SIO_000300: 1.391e1

MQRankSum
type: SiteQuality
SIO_000300: -1.473e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.740704637237154e-5
allele num: 57448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.036176e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
all individuals: 6940
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 1

South Asian
type: Population
allele count: 17
allele frequency: 1.352426412092283e-3
allele num: 12570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.373626373626374e-3
allele num: 728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.471860570079506e-5
allele num: 57606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.043214e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

GenotypeQuality
all individuals: 1547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4393
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GenotypeQuality
all individuals: 208
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GenotypeQuality
all individuals: 5837
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6702
bin: 3.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7658
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8704
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58336
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.039e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.109564e6

GenotypeQuality
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variant carriers: 8

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.371365880416895e-4
allele num: 58336
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8704
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

FS
type: SiteQuality
SIO_000300: 1.039e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 1.109564e6

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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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8710
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10014
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.71051281174096e-5
allele num: 58462
num of homozygotes: 0

South Asian
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allele frequency: 2.304855562384757e-4
allele num: 13016
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4992
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.124435e6

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

South Asian
type: Population
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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Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.290655653071761e-4
allele num: 7748
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59066
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.545e-1

MQRankSum
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.688e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 9.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.1e-1

DP
type: SiteQuality
SIO_000300: 1.163107e6

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5064
num of homozygotes: 0

Other
type: Population
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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: 59074
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
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African
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allele count: 1
allele frequency: 1.132502831257078e-4
allele num: 8830
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.249e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.082e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.177138e6

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.563e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5112
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.681520094165125e-5
allele num: 59470
num of homozygotes: 0

Latino
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South Asian
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allele count: 0
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InbreedingCoeff
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SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 1.752e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.334667200213418e-5
allele num: 59976
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Other
type: Population
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allele num: 780
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African
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Latino
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South Asian
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
type: SiteQuality
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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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European (Non-Finnish)
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Latino
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African
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South Asian
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East Asian
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Other
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European (Finnish)
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
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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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African
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Latino
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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FS
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QD
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VQSLOD
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ClippingRankSum
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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European (Non-Finnish)
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allele num: 60826
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Latino
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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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Other
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MQ
type: SiteQuality
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
type: SiteQuality
SIO_000300: -2.118e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

GenotypeQuality
all individuals: 6824
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26776
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.635750973271829e-5
allele num: 61134
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 4.576e0

VQSLOD
type: SiteQuality
SIO_000300: -2.726e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.290103e6

QD
type: SiteQuality
SIO_000300: 2.772e1

GenotypeQuality
all individuals: 28811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 676
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.229407425620851e-4
allele num: 8134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62130
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.032e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.458e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

DP
type: SiteQuality
SIO_000300: 1.335683e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.735e0

GenotypeQuality
all individuals: 805
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 678
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6671
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.838235294117647e-4
allele num: 10880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

DP
type: SiteQuality
SIO_000300: 1.385511e6

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4