19-55385789-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385789
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385789
    reference: chr 19
allele count: 3
allele frequency: 2.471739775236463e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+10A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+10A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-55385796-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385796
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385796
    reference: chr 19
allele count: 5
allele frequency: 4.119702063146793e-5
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+17A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+17A>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

19-55385797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385797
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385797
    reference: chr 19
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+18A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

19-55385798-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385798
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385798
    reference: chr 19
allele count: 37
allele frequency: 3.048730245051993e-4
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+19G>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-55385800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385800
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385800
    reference: chr 19
allele count: 78
allele frequency: 6.427370710966083e-4
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+21G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+21G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

19-55385804-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385804
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385804
    reference: chr 19
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+25T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+25T>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-55385813-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385813
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385813
    reference: chr 19
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+34A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+34A>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

19-55385814-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385814
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385814
    reference: chr 19
allele count: 9
allele frequency: 7.417908479493604e-5
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+35G>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9969
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

19-55385816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385816
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385816
    reference: chr 19
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+37T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-55385818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385818
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385818
    reference: chr 19
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+39G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9053
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-55385826-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55385826
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55385826
    reference: chr 19
allele count: 2
allele frequency: 1.650192247396822e-5
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.34+47C>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

19-55386736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386736
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386736
    reference: chr 19
allele count: 10
allele frequency: 8.272393368849475e-5
allele num: 120884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+957G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-50G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

19-55386738-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386738
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386738
    reference: chr 19
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-48A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+959A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16388
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

19-55386743-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386743
    reference: chr 19
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+964T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-43T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

19-55386756-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386756
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386756
    reference: chr 19
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+977C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-30C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

19-55386757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386757
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386757
    reference: chr 19
allele count: 2
allele frequency: 1.652291728627607e-5
allele num: 121044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-29T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+978T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+978T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

19-55386767-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386767
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386767
    reference: chr 19
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-19A>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+988A>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

19-55386772-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386772
    reference: chr 19
allele count: 7
allele frequency: 5.777198223924203e-5
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+993T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-14T>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

19-55386775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386775
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386775
    reference: chr 19
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-11C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+996C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

19-55386777-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386777
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386777
    reference: chr 19
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+998C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-9C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+998C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-55386778-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386778
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386778
    reference: chr 19
allele count: 7
allele frequency: 5.775577557755776e-5
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+999T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-8T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+999T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.35-8T>C
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

19-55386779-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386779
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386778
    reference: chr 19
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-5delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-5delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-5delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-5delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1002delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-5delT
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-5delT
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.35-5delT
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: CT
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

19-55386782-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386782
    reference: chr 19
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1003C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.35-4C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.35-4C>G
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

19-55386789-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386789
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386789
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.38T>C
  hgvsp: ENSP00000473814.1:p.Leu13Pro
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.38T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.38T>C
  hgvsp: ENSP00000375605.3:p.Leu13Pro
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.38T>C
  hgvsp: ENSP00000338257.4:p.Leu13Pro
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.38T>C
  hgvsp: ENSP00000347714.3:p.Leu13Pro
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.38T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1010T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16396
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu13Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

19-55386792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386792
    reference: chr 19
allele count: 2
allele frequency: 1.649266900862567e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.41G>A
  hgvsp: ENSP00000473814.1:p.Cys14Tyr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.41G>A
  hgvsp: ENSP00000375605.3:p.Cys14Tyr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.41G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.41G>A
  hgvsp: ENSP00000347714.3:p.Cys14Tyr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.41G>A
  hgvsp: ENSP00000338257.4:p.Cys14Tyr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1013G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.41G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16423
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys14Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

19-55386792-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386792
    reference: chr 19
allele count: 63
allele frequency: 5.195190737717084e-4
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.41G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.41G>C
  hgvsp: ENSP00000347714.3:p.Cys14Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.41G>C
  hgvsp: ENSP00000375605.3:p.Cys14Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.41G>C
  hgvsp: ENSP00000338257.4:p.Cys14Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.41G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1013G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.41G>C
  hgvsp: ENSP00000473814.1:p.Cys14Ser
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16423
  bin: 9.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys14Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-55386802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386802
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386802
    reference: chr 19
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.51G>A
  hgvsp: ENST00000355524.3:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.51G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.51G>A
  hgvsp: ENST00000391725.3:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.51G>A
  hgvsp: ENST00000345937.4:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.51G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.51G>A
  hgvsp: ENST00000469767.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1023G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln17Gln
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

19-55386805-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386805
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386805
    reference: chr 19
allele count: 4
allele frequency: 3.297881111385935e-5
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.54G>A
  hgvsp: ENST00000355524.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.54G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.54G>A
  hgvsp: ENST00000345937.4:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.54G>A
  hgvsp: ENST00000391725.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1026G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.54G>A
  hgvsp: ENST00000469767.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.54G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16393
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg18Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

19-55386805-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386805
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386805
    reference: chr 19
allele count: 6
allele frequency: 4.946821667078902e-5
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.54G>C
  hgvsp: ENSP00000375605.3:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.54G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.54G>C
  hgvsp: ENSP00000473814.1:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.54G>C
  hgvsp: ENSP00000347714.3:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.54G>C
  hgvsp: ENSP00000338257.4:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.54G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1026G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1026G>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg18Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

19-55386806-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386806
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386806
    reference: chr 19
allele count: 7
allele frequency: 5.771387111668096e-5
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.55A>G
  hgvsp: ENSP00000338257.4:p.Ile19Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.55A>G
  hgvsp: ENSP00000347714.3:p.Ile19Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.55A>G
  hgvsp: ENSP00000375605.3:p.Ile19Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.55A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.55A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.55A>G
  hgvsp: ENSP00000473814.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1027A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile19Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

19-55386818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386818
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386818
    reference: chr 19
allele count: 17
allele frequency: 1.401807507091497e-4
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.67G>A
  hgvsp: ENSP00000347714.3:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.67G>A
  hgvsp: ENSP00000338257.4:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.67G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.67G>A
  hgvsp: ENSP00000375605.3:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.67G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.67G>A
  hgvsp: ENSP00000473814.1:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1039G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu23Lys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-55386821-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386821
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386821
    reference: chr 19
allele count: 97
allele frequency: 7.998680629999176e-4
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70G>A
  hgvsp: ENSP00000347714.3:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70G>A
  hgvsp: ENSP00000473814.1:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1042G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70G>A
  hgvsp: ENSP00000375605.3:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70G>A
  hgvsp: ENSP00000338257.4:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16433
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly24Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

19-55386822-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386822
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386822
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1043G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+1G>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16406
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.70+1G>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

19-55386824-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386824
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386824
    reference: chr 19
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1045A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+3A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.70+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-55386831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386831
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386831
    reference: chr 19
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1052C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+10C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-55386832-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386832
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386832
    reference: chr 19
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1053T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+11T>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16406
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-55386837-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386837
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386837
    reference: chr 19
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1058A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+16A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16406
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

19-55386843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386843
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386843
    reference: chr 19
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1064C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+22C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-55386845-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386845
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386845
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1066C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+24C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16407
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS

19-55386852-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386852
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386852
    reference: chr 19
allele count: 2
allele frequency: 1.649566164098842e-5
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1073T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+31T>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16409
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

19-55386854-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386854
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386854
    reference: chr 19
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+33T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1075T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16408
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-55386858-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386858
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386858
    reference: chr 19
allele count: 4875
allele frequency: 4.022011748399446e-2
allele num: 121208
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+37C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1079C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 2.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 4.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 8.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 5.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 7.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 7.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 6.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 18220
  bin: 9.75e1
  variant carriers: 2937
genotype quality: GenotypeQuality
num of homozygotes: 126
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-55386860-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386860
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386860
    reference: chr 19
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+39C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1081C>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-55386860-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386860
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386860
    reference: chr 19
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1081C>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+39C>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

19-55386869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55386869
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55386869
    reference: chr 19
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.44+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.34+1090G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.70+48G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17038
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

19-55396606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396606
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396606
    reference: chr 19
allele count: 1
allele frequency: 8.847834934791456e-6
allele num: 113022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2768C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-41C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-41C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-55396613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396613
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396613
    reference: chr 19
allele count: 76129
allele frequency: 6.491217598908595e-1
allele num: 117280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2761G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-34G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-34G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 1.75e1
  variant carriers: 7652
genotype depth: GenotypeDepth
  all individuals: 13436
  bin: 2.25e1
  variant carriers: 10434
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 584
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 2.75e1
  variant carriers: 10394
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 7.5e0
  variant carriers: 893
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 3.75e1
  variant carriers: 4796
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.25e1
  variant carriers: 916
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 4.75e1
  variant carriers: 1575
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 4.25e1
  variant carriers: 2754
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 1.25e1
  variant carriers: 3658
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 3.25e1
  variant carriers: 7693
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
num of homozygotes: 24895
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

19-55396619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396619
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396619
    reference: chr 19
allele count: 1
allele frequency: 8.433836552247617e-6
allele num: 118570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2755C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-28C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-28C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

19-55396624-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396624
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396624
    reference: chr 19
allele count: 1
allele frequency: 8.419492809753141e-6
allele num: 118772
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2750G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-23G>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-23G>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13208
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-55396625-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396625
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396625
    reference: chr 19
allele count: 1
allele frequency: 8.417366710998132e-6
allele num: 118802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2749T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-22T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-22T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

19-55396626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396626
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396626
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 118826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2748C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-21C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-21C>T
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-55396637-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396637
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396637
    reference: chr 19
allele count: 4
allele frequency: 3.349578790467099e-5
allele num: 119418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.149-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.35-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.35-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.71-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.35-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.35-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.71-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.71-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2737T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.35-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.71-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.123-10T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.149-10T>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20009
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

19-55396657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396657
    reference: chr 19
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.45C>T
  hgvsp: ENST00000391726.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.81C>T
  hgvsp: ENST00000469767.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2717C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.81C>T
  hgvsp: ENST00000355524.3:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.45C>T
  hgvsp: ENST00000391724.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.81C>T
  hgvsp: ENST00000345937.4:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.133C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.45C>T
  hgvsp: ENST00000359272.4:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.159C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.45C>T
  hgvsp: ENST00000391723.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.45C>T
  hgvsp: ENST00000488066.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.159C>T
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.81C>T
  hgvsp: ENST00000391725.3:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro27Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

19-55396658-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396658
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396658
    reference: chr 19
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2716A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.46A>G
  hgvsp: ENSP00000474512.1:p.Met16Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.82A>G
  hgvsp: ENSP00000473814.1:p.Met28Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.82A>G
  hgvsp: ENSP00000338257.4:p.Met28Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.46A>G
  hgvsp: ENSP00000375603.3:p.Met16Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.46A>G
  hgvsp: ENSP00000375604.3:p.Met16Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.82A>G
  hgvsp: ENSP00000347714.3:p.Met28Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.160A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.46A>G
  hgvsp: ENSP00000375606.3:p.Met16Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.160A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.134A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.46A>G
  hgvsp: ENSP00000352218.4:p.Met16Val
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.82A>G
  hgvsp: ENSP00000375605.3:p.Met28Val
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10615
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met28Val
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: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-55396667-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396667
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396667
    reference: chr 19
allele count: 2
allele frequency: 1.651991475723985e-5
allele num: 121066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.91A>C
  hgvsp: ENSP00000375605.3:p.Ile31Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.91A>C
  hgvsp: ENSP00000338257.4:p.Ile31Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.91A>C
  hgvsp: ENSP00000347714.3:p.Ile31Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.55A>C
  hgvsp: ENSP00000375604.3:p.Ile19Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.55A>C
  hgvsp: ENSP00000375603.3:p.Ile19Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.55A>C
  hgvsp: ENSP00000375606.3:p.Ile19Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.55A>C
  hgvsp: ENSP00000352218.4:p.Ile19Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.91A>C
  hgvsp: ENSP00000473814.1:p.Ile31Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.55A>C
  hgvsp: ENSP00000474512.1:p.Ile19Leu
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.169A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.143A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2707A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.169A>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile31Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

19-55396668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396668
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396668
    reference: chr 19
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.56T>C
  hgvsp: ENSP00000375603.3:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.56T>C
  hgvsp: ENSP00000375604.3:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.56T>C
  hgvsp: ENSP00000474512.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.92T>C
  hgvsp: ENSP00000338257.4:p.Ile31Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2706T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.56T>C
  hgvsp: ENSP00000352218.4:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.92T>C
  hgvsp: ENSP00000347714.3:p.Ile31Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.170T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.92T>C
  hgvsp: ENSP00000375605.3:p.Ile31Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.92T>C
  hgvsp: ENSP00000473814.1:p.Ile31Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.170T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.144T>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.56T>C
  hgvsp: ENSP00000375606.3:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile31Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

19-55396668-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396668
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396668
    reference: chr 19
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2706T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.92T>G
  hgvsp: ENSP00000375605.3:p.Ile31Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.56T>G
  hgvsp: ENSP00000375603.3:p.Ile19Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.92T>G
  hgvsp: ENSP00000338257.4:p.Ile31Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.92T>G
  hgvsp: ENSP00000347714.3:p.Ile31Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.92T>G
  hgvsp: ENSP00000473814.1:p.Ile31Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.56T>G
  hgvsp: ENSP00000375604.3:p.Ile19Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.170T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.170T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.56T>G
  hgvsp: ENSP00000375606.3:p.Ile19Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.144T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.56T>G
  hgvsp: ENSP00000352218.4:p.Ile19Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.56T>G
  hgvsp: ENSP00000474512.1:p.Ile19Arg
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10848
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile31Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

19-55396669-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396669
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396669
    reference: chr 19
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.57A>G
  hgvsp: ENSP00000375603.3:p.Ile19Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.57A>G
  hgvsp: ENSP00000352218.4:p.Ile19Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.171A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.57A>G
  hgvsp: ENSP00000375604.3:p.Ile19Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.57A>G
  hgvsp: ENSP00000474512.1:p.Ile19Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.93A>G
  hgvsp: ENSP00000347714.3:p.Ile31Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.145A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.57A>G
  hgvsp: ENSP00000375606.3:p.Ile19Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.93A>G
  hgvsp: ENSP00000375605.3:p.Ile31Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.93A>G
  hgvsp: ENSP00000338257.4:p.Ile31Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2705A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.93A>G
  hgvsp: ENSP00000473814.1:p.Ile31Met
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.171A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15580
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile31Met
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-55396672-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396672
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396672
    reference: chr 19
allele count: 9
allele frequency: 7.430156528630869e-5
allele num: 121128
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.96T>G
  hgvsp: ENST00000355524.3:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.60T>G
  hgvsp: ENST00000488066.1:c.60T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.96T>G
  hgvsp: ENST00000345937.4:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.148T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.174T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2702T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.60T>G
  hgvsp: ENST00000359272.4:c.60T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.60T>G
  hgvsp: ENST00000391726.3:c.60T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.60T>G
  hgvsp: ENST00000391723.3:c.60T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.96T>G
  hgvsp: ENST00000469767.1:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.174T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.60T>G
  hgvsp: ENST00000391724.3:c.60T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.96T>G
  hgvsp: ENST00000391725.3:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser32Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-55396677-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396677
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396677
    reference: chr 19
allele count: 185
allele frequency: 1.52647820849217e-3
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.179A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.65A>C
  hgvsp: ENSP00000352218.4:p.Lys22Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.101A>C
  hgvsp: ENSP00000375605.3:p.Lys34Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.101A>C
  hgvsp: ENSP00000347714.3:p.Lys34Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.101A>C
  hgvsp: ENSP00000338257.4:p.Lys34Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.153A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.65A>C
  hgvsp: ENSP00000375606.3:p.Lys22Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.65A>C
  hgvsp: ENSP00000375603.3:p.Lys22Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.65A>C
  hgvsp: ENSP00000474512.1:p.Lys22Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.179A>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.101A>C
  hgvsp: ENSP00000473814.1:p.Lys34Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.65A>C
  hgvsp: ENSP00000375604.3:p.Lys22Thr
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2697A>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 15653
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys34Thr
num of homozygotes: 2
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

19-55396677-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396677
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396677
    reference: chr 19
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.65A>G
  hgvsp: ENSP00000375603.3:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.101A>G
  hgvsp: ENSP00000473814.1:p.Lys34Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.65A>G
  hgvsp: ENSP00000375606.3:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.65A>G
  hgvsp: ENSP00000352218.4:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.101A>G
  hgvsp: ENSP00000338257.4:p.Lys34Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.179A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.153A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2697A>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.65A>G
  hgvsp: ENSP00000474512.1:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.65A>G
  hgvsp: ENSP00000375604.3:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.101A>G
  hgvsp: ENSP00000347714.3:p.Lys34Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.101A>G
  hgvsp: ENSP00000375605.3:p.Lys34Arg
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.179A>G
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys34Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/19-55396680-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396680
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396680
    reference: chr 19
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.182C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.182C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.104C>A
  hgvsp: ENSP00000375605.3:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.156C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.104C>A
  hgvsp: ENSP00000473814.1:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.68C>A
  hgvsp: ENSP00000375603.3:p.Ser23Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.68C>A
  hgvsp: ENSP00000375604.3:p.Ser23Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.68C>A
  hgvsp: ENSP00000375606.3:p.Ser23Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.104C>A
  hgvsp: ENSP00000338257.4:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.68C>A
  hgvsp: ENSP00000352218.4:p.Ser23Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.68C>A
  hgvsp: ENSP00000474512.1:p.Ser23Ter
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2694C>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.104C>A
  hgvsp: ENSP00000347714.3:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser35Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-55396700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396700
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396700
    reference: chr 19
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.88G>A
  hgvsp: ENSP00000352218.4:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.88G>A
  hgvsp: ENSP00000375606.3:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.88G>A
  hgvsp: ENSP00000375604.3:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.176G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.88G>A
  hgvsp: ENSP00000474512.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.124G>A
  hgvsp: ENSP00000473814.1:p.Asp42Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.88G>A
  hgvsp: ENSP00000375603.3:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.124G>A
  hgvsp: ENSP00000347714.3:p.Asp42Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.202G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.202G>A
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.124G>A
  hgvsp: ENSP00000338257.4:p.Asp42Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.124G>A
  hgvsp: ENSP00000375605.3:p.Asp42Asn
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2674G>A
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp42Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

19-55396704-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396704
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396704
    reference: chr 19
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.92G>C
  hgvsp: ENSP00000375604.3:p.Gly31Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.206G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.92G>C
  hgvsp: ENSP00000375603.3:p.Gly31Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.180G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.206G>C
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.128G>C
  hgvsp: ENSP00000375605.3:p.Gly43Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.128G>C
  hgvsp: ENSP00000338257.4:p.Gly43Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.92G>C
  hgvsp: ENSP00000375606.3:p.Gly31Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.92G>C
  hgvsp: ENSP00000474512.1:p.Gly31Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.92G>C
  hgvsp: ENSP00000352218.4:p.Gly31Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.128G>C
  hgvsp: ENSP00000473814.1:p.Gly43Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.128G>C
  hgvsp: ENSP00000347714.3:p.Gly43Ala
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2670G>C
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly43Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

19-55396708-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396708
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396708
    reference: chr 19
allele count: 12
allele frequency: 9.887447884910107e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.132T>G
  hgvsp: ENST00000345937.4:c.132T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.96T>G
  hgvsp: ENST00000391723.3:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.96T>G
  hgvsp: ENST00000359272.4:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.210T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.184T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.210T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.132T>G
  hgvsp: ENST00000391725.3:c.132T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.96T>G
  hgvsp: ENST00000391726.3:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.96T>G
  hgvsp: ENST00000488066.1:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.96T>G
  hgvsp: ENST00000391724.3:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.132T>G
  hgvsp: ENST00000469767.1:c.132T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2666T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.132T>G
  hgvsp: ENST00000355524.3:c.132T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser44Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

19-55396710-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55396710
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55396710
    reference: chr 19
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375604
  ensembl transcript: ENST00000391724
  gene symbol: FCAR
  hgvsc: ENST00000391724.3:c.98T>G
  hgvsp: ENSP00000375604.3:p.Val33Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000471750
  gene symbol: FCAR
  hgvsc: ENST00000471750.2:n.212T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375605
  ensembl transcript: ENST00000391725
  gene symbol: FCAR
  hgvsc: ENST00000391725.3:c.134T>G
  hgvsp: ENSP00000375605.3:p.Val45Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338058
  ensembl transcript: ENST00000353758
  gene symbol: FCAR
  hgvsc: ENST00000353758.4:c.35-2664T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000472634
  gene symbol: FCAR
  hgvsc: ENST00000472634.2:n.186T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375603
  ensembl transcript: ENST00000391723
  gene symbol: FCAR
  hgvsc: ENST00000391723.3:c.98T>G
  hgvsp: ENSP00000375603.3:p.Val33Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000473814
  ensembl transcript: ENST00000469767
  gene symbol: FCAR
  hgvsc: ENST00000469767.1:c.134T>G
  hgvsp: ENSP00000473814.1:p.Val45Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186431
  ensembl transcript: ENST00000482092
  gene symbol: FCAR
  hgvsc: ENST00000482092.2:n.212T>G
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000352218
  ensembl transcript: ENST00000359272
  gene symbol: FCAR
  hgvsc: ENST00000359272.4:c.98T>G
  hgvsp: ENSP00000352218.4:p.Val33Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000474512
  ensembl transcript: ENST00000488066
  gene symbol: FCAR
  hgvsc: ENST00000488066.1:c.98T>G
  hgvsp: ENSP00000474512.1:p.Val33Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000347714
  ensembl transcript: ENST00000355524
  gene symbol: FCAR
  hgvsc: ENST00000355524.3:c.134T>G
  hgvsp: ENSP00000347714.3:p.Val45Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000338257
  ensembl transcript: ENST00000345937
  gene symbol: FCAR
  hgvsc: ENST00000345937.4:c.134T>G
  hgvsp: ENSP00000338257.4:p.Val45Gly
  variant of: http://identifiers.org/hgnc/3608
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186431
  ensembl protein: ENSP00000375606
  ensembl transcript: ENST00000391726
  gene symbol: FCAR
  hgvsc: ENST00000391726.3:c.98T>G
  hgvsp: ENSP00000375606.3:p.Val33Gly
  variant of: http://identifiers.org/hgnc/3608
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val45Gly
num of homozygotes: 0
population: African
reference allele: T

GenotypeDepth
all individuals: 1554
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1386
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4936
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27527
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5069
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.215e1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e-1

FS
type: SiteQuality
SIO_000300: 2.989e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.229e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.751e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.697795e6

GenotypeDepth
all individuals: 7148
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6490
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2033
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4478
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2528
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5073
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27524
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4734
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496027105634013e-5
allele num: 66702
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.697234e6

FS
type: SiteQuality
SIO_000300: 6.888e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

QD
type: SiteQuality
SIO_000300: 1.688e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

GenotypeDepth
all individuals: 9084
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1508
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4938
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8738
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27521
bin: 9.75e1
variant carriers: 3

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

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

GenotypeQuality
all individuals: 5064
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2528
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 2.363e0

DP
type: SiteQuality
SIO_000300: 2.696707e6

MQRankSum
type: SiteQuality
SIO_000300: 8.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 440
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1333
bin: 6.75e1
variant carriers: 6

GenotypeDepth
all individuals: 1384
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2537
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8749
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27522
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4479
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5062
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2528
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4732
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 2.998590662388677e-4
allele num: 66698
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.295560545862843e-3
allele num: 11578
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.89e0

DP
type: SiteQuality
SIO_000300: 2.696583e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.413e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.213e0

GenotypeDepth
all individuals: 6470
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1381
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8693
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27498
bin: 9.75e1
variant carriers: 76

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.094518411898764e-3
allele num: 66696
num of homozygotes: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.694998e6

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3101
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9090
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4485
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2533
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2535
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.533e1

FS
type: SiteQuality
SIO_000300: 1.712e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.297e0

DP
type: SiteQuality
SIO_000300: 2.691771e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.676e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9068
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6313
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4480
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variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4939
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8184
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27446
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.705e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

FS
type: SiteQuality
SIO_000300: 3.32e0

DP
type: SiteQuality
SIO_000300: 2.684025e6

GenotypeDepth
all individuals: 1365
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10212
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
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variant carriers: 0

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

GenotypeQuality
all individuals: 8209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4479
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27451
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 9
allele frequency: 5.453223460979156e-4
allele num: 16504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 3.493e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.68391e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

GenotypeDepth
all individuals: 583
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 624
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2018
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4931
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2525
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4935
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27438
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999670036296008e-5
allele num: 66674
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 6.446e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 1.645e1

DP
type: SiteQuality
SIO_000300: 2.681189e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 10037
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4475
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4702
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4910
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.173e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 3.522e0

DP
type: SiteQuality
SIO_000300: 2.678034e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.27e-1

GenotypeDepth
all individuals: 436
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 770
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 918
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4618
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5623
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4455
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.331e-1

MQRankSum
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SIO_000300: -1.8e-2

BaseQRankSum
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SIO_000300: -2.115e0

InbreedingCoeff
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SIO_000300: 1.3e-3

DP
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SIO_000300: 2.659949e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.161429451632779e-5
allele num: 16230
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.508837321149453e-5
allele num: 66536
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.848514e6

ReadPosRankSum
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SIO_000300: 5.04e-1

MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: 4.62e0

MQ
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SIO_000300: 5.984e1

ClippingRankSum
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SIO_000300: -5.72e-1

FS
type: SiteQuality
SIO_000300: 7.28e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.147792942333702e-5
allele num: 16266
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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DP
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SIO_000300: 4.849203e6

ReadPosRankSum
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SIO_000300: 6.54e-1

QD
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VQSLOD
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SIO_000300: 1.34e0

MQRankSum
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SIO_000300: -2.76e-1

ClippingRankSum
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SIO_000300: -3.44e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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SIO_000300: 1.525e1

DP
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SIO_000300: 4.852537e6

GenotypeDepth
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

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

Other
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African
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allele num: 10382
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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African
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South Asian
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

European (Non-Finnish)
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Other
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East Asian
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African
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European (Finnish)
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Latino
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allele frequency: 6.049083995852057e-4
allele num: 11572
num of homozygotes: 0

DP
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SIO_000300: 4.8656e6

BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.67e-1

ReadPosRankSum
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SIO_000300: 1.5e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 4.885e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

MQ
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SIO_000300: 5.913e1

MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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SIO_000300: 7.07e-2

ReadPosRankSum
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QD
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SIO_000300: 8.039999999999999e0

ClippingRankSum
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SIO_000300: -1.018e0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -1.544e0

VQSLOD
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MQRankSum
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MQ
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QD
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DP
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SIO_000300: 4.866443e6

ReadPosRankSum
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SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.37e-2

BaseQRankSum
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SIO_000300: 5.34e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.780346820809249e-4
allele num: 8650
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

MQRankSum
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SIO_000300: -4.91e-1

VQSLOD
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SIO_000300: 1.15e0

InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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FS
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SIO_000300: 2.562e0

MQ
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SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 4.866845e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele num: 11572
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 4.46e-1

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

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

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

African
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allele count: 55
allele frequency: 5.29457065845206e-3
allele num: 10388
num of homozygotes: 0

Latino
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allele count: 7
allele frequency: 6.049083995852057e-4
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16474
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
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allele num: 906
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DP
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FS
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MQRankSum
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.59e-1

BaseQRankSum
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SIO_000300: 4.46e-1

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

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

South Asian
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allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
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SIO_000300: 5.702e1

ReadPosRankSum
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SIO_000300: -6.830000000000001e-1

MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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SIO_000300: -2.317e0

QD
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SIO_000300: 9.529999999999999e0

ClippingRankSum
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SIO_000300: -8.5e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.999340072592015e-5
allele num: 66674
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
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num of homozygotes: 0

Other
type: Population
allele count: 0
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MQRankSum
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SIO_000300: 1.41e-1

VQSLOD
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QD
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MQ
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InbreedingCoeff
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FS
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SIO_000300: 5.21e-1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.95e-1

ClippingRankSum
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SIO_000300: -5.91e-1

DP
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SIO_000300: 4.868151e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

South Asian
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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: 0.0e0
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Latino
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allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.849114703618168e-4
allele num: 10392
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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FS
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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African
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Latino
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num of homozygotes: 0

European (Finnish)
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South Asian
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Other
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 14

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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Other
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DP
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

South Asian
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allele count: 96
allele frequency: 5.825949751183396e-3
allele num: 16478
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.84e-1

DP
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SIO_000300: 4.872365e6

ClippingRankSum
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SIO_000300: -2.32e-1

MQRankSum
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MQ
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SIO_000300: 5.932e1

ReadPosRankSum
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SIO_000300: 5.76e-1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

FS
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SIO_000300: 5.24e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

VQSLOD
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SIO_000300: 1.92e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
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SIO_000300: 4.868829e6

MQRankSum
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SIO_000300: -6.879999999999999e-1

FS
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

QD
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ClippingRankSum
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SIO_000300: 2.5e-1

VQSLOD
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SIO_000300: 5.2e-2

BaseQRankSum
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SIO_000300: -1.766e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4164
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 4.868735e6

FS
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SIO_000300: 5.75e0

MQRankSum
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SIO_000300: 1.37e-1

BaseQRankSum
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SIO_000300: 3.87e0

ClippingRankSum
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SIO_000300: -1.198e0

VQSLOD
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QD
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SIO_000300: 1.239e1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
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SIO_000300: 2.16e0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.811e0

DP
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SIO_000300: 4.868179e6

MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: 3.61e-1

VQSLOD
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SIO_000300: -3.34e0

InbreedingCoeff
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SIO_000300: 1.0e-4

FS
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SIO_000300: 1.5045e1

QD
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SIO_000300: 9.92e0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

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

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

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

Latino
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num of homozygotes: 0

African
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allele frequency: 9.63020030816641e-5
allele num: 10384
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BaseQRankSum
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QD
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

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

African
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South Asian
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allele num: 16468
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

MQ
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SIO_000300: 5.97e1

VQSLOD
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SIO_000300: 5.24e-1

MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 4.71e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
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

FS
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SIO_000300: 7.24e0

ClippingRankSum
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SIO_000300: 2.38e0

InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.988e1

VQSLOD
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SIO_000300: -8.463000000000001e-1

ReadPosRankSum
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SIO_000300: -1.744e0

QD
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SIO_000300: 1.397e1

DP
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SIO_000300: 4.86456e6

MQRankSum
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SIO_000300: 9.62e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

VQSLOD
type: SiteQuality
SIO_000300: -1.012e-1

FS
type: SiteQuality
SIO_000300: 1.327e0

MQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

InbreedingCoeff
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SIO_000300: 1.04e-2

MQ
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SIO_000300: 5.884e1

QD
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SIO_000300: 1.247e1

ReadPosRankSum
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SIO_000300: 1.0e-3

DP
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SIO_000300: 4.863464e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

GenotypeDepth
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bin: 8.75e1
variant carriers: 208

GenotypeDepth
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variant carriers: 193

GenotypeDepth
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variant carriers: 112

GenotypeQuality
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GenotypeQuality
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variant carriers: 4737

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 46
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GenotypeQuality
all individuals: 120
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variant carriers: 0

Other
type: Population
allele count: 48
allele frequency: 5.309734513274336e-2
allele num: 904
num of homozygotes: 2

Latino
type: Population
allele count: 282
allele frequency: 2.436495593571799e-2
allele num: 11574
num of homozygotes: 6

African
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allele count: 596
allele frequency: 5.74291771054153e-2
allele num: 10378
num of homozygotes: 20

European (Non-Finnish)
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allele count: 2322
allele frequency: 3.483766428614295e-2
allele num: 66652
num of homozygotes: 48

East Asian
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allele count: 681
allele frequency: 7.872832369942197e-2
allele num: 8650
num of homozygotes: 30

European (Finnish)
type: Population
allele count: 211
allele frequency: 3.1902026005443e-2
allele num: 6614
num of homozygotes: 3

South Asian
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allele count: 735
allele frequency: 4.471890971039182e-2
allele num: 16436
num of homozygotes: 17

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
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SIO_000300: -8.3e-2

DP
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SIO_000300: 5.01903e6

MQRankSum
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SIO_000300: 1.67e-1

FS
type: SiteQuality
SIO_000300: 3.565e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
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SIO_000300: 1.28e-2

VQSLOD
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SIO_000300: 2.16e0

ReadPosRankSum
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SIO_000300: 2.01e-1

QD
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SIO_000300: 1.245e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 345
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -2.311e0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

African
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allele count: 0
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South Asian
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InbreedingCoeff
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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MQ
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SIO_000300: 5.974e1

QD
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SIO_000300: 1.252e1

VQSLOD
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ReadPosRankSum
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SIO_000300: 6.3e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

South Asian
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allele count: 0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10356
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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Other
type: Population
allele count: 0
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Latino
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.029e0

FS
type: SiteQuality
SIO_000300: 1.1208e1

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2206
bin: 8.25e1
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GenotypeQuality
all individuals: 15596
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.108330963889678e-5
allele num: 14068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63232
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.578e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

DP
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SIO_000300: 1.353035e6

VQSLOD
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SIO_000300: 2.02e-1

ClippingRankSum
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SIO_000300: -1.14e-1

InbreedingCoeff
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SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

GenotypeDepth
all individuals: 241
bin: 6.75e1
variant carriers: 235

GenotypeDepth
all individuals: 110
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variant carriers: 104

GenotypeDepth
all individuals: 361
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variant carriers: 349

GenotypeQuality
all individuals: 1127
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variant carriers: 668

GenotypeQuality
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bin: 1.25e1
variant carriers: 131

GenotypeQuality
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variant carriers: 82

GenotypeQuality
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variant carriers: 33157

GenotypeQuality
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variant carriers: 939

GenotypeQuality
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variant carriers: 198

GenotypeQuality
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variant carriers: 676

GenotypeQuality
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GenotypeQuality
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variant carriers: 1524

GenotypeQuality
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GenotypeQuality
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variant carriers: 344

GenotypeQuality
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variant carriers: 2005

GenotypeQuality
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variant carriers: 339

GenotypeQuality
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variant carriers: 2102

GenotypeQuality
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variant carriers: 2090

GenotypeQuality
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bin: 5.75e1
variant carriers: 1055

GenotypeQuality
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bin: 8.25e1
variant carriers: 1865

GenotypeQuality
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bin: 4.75e1
variant carriers: 1449

GenotypeQuality
all individuals: 1032
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variant carriers: 977

GenotypeQuality
all individuals: 1360
bin: 7.25e1
variant carriers: 1155

Other
type: Population
allele count: 550
allele frequency: 6.207674943566591e-1
allele num: 886
num of homozygotes: 181

East Asian
type: Population
allele count: 5412
allele frequency: 6.523625843780135e-1
allele num: 8296
num of homozygotes: 1758

European (Non-Finnish)
type: Population
allele count: 43857
allele frequency: 6.751801219286901e-1
allele num: 64956
num of homozygotes: 14742

European (Finnish)
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allele count: 3991
allele frequency: 6.208774113254512e-1
allele num: 6428
num of homozygotes: 1255

Latino
type: Population
allele count: 5309
allele frequency: 4.737640549705515e-1
allele num: 11206
num of homozygotes: 1268

South Asian
type: Population
allele count: 9922
allele frequency: 6.383991764251705e-1
allele num: 15542
num of homozygotes: 3168

African
type: Population
allele count: 7088
allele frequency: 7.112181416817178e-1
allele num: 9966
num of homozygotes: 2523

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 2.429e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 2.79e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 1.65187e6

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4541
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15692
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523832744118006e-5
allele num: 65624
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-1

FS
type: SiteQuality
SIO_000300: 2.992e0

QD
type: SiteQuality
SIO_000300: 3.178e1

DP
type: SiteQuality
SIO_000300: 1.684247e6

BaseQRankSum
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SIO_000300: -1.387e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.664e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeDepth
all individuals: 378
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 3679
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1017
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 2005
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GenotypeQuality
all individuals: 10700
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GenotypeQuality
all individuals: 3732
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GenotypeQuality
all individuals: 4646
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522209029743965e-5
allele num: 65694
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.478e1

DP
type: SiteQuality
SIO_000300: 1.702445e6

BaseQRankSum
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SIO_000300: -1.793e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeDepth
all individuals: 13287
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 16589
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GenotypeQuality
all individuals: 1443
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GenotypeQuality
all individuals: 87
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1530
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6914
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GenotypeQuality
all individuals: 2014
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variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.960159362549801e-5
allele num: 10040
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65712
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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FS
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MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.545e1

BaseQRankSum
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SIO_000300: 1.9e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17317
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65720
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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SIO_000300: -9.788e-1

FS
type: SiteQuality
SIO_000300: 1.953e0

ReadPosRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.710173e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10786
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.96589331746976e-4
allele num: 10086
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.11e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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Latino
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allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

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

East Asian
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allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

InbreedingCoeff
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BaseQRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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DP
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SIO_000300: 1.798792e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004446580939791e-5
allele num: 66568
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
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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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num of homozygotes: 0

East Asian
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South Asian
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African
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6598
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Other
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South Asian
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African
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European (Finnish)
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East Asian
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Latino
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Latino
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num of homozygotes: 0

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

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

East Asian
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allele count: 9
allele frequency: 1.043357291908185e-3
allele num: 8626
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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QD
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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SIO_000300: 5.01e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
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SIO_000300: 3.6e0

DP
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SIO_000300: 1.810666e6

ClippingRankSum
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SIO_000300: 5.5e-1

BaseQRankSum
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SIO_000300: -1.298e0

GenotypeDepth
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variant carriers: 21

GenotypeDepth
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variant carriers: 15

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 10

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 183

African
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allele count: 161
allele frequency: 1.55165767154973e-2
allele num: 10376
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.5036768016328e-5
allele num: 66634
num of homozygotes: 0

Latino
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allele count: 19
allele frequency: 1.645021645021645e-3
allele num: 11550
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.441e1

ClippingRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.971e1

ReadPosRankSum
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SIO_000300: 3.63e-1

MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
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 count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

VQSLOD
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SIO_000300: 4.14e0

InbreedingCoeff
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SIO_000300: 9.599999999999999e-3

BaseQRankSum
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SIO_000300: 2.78e0

FS
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SIO_000300: 5.639999999999999e-1

ClippingRankSum
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SIO_000300: 1.71e-1

MQRankSum
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SIO_000300: 3.88e-1

QD
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SIO_000300: 1.441e1

ReadPosRankSum
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SIO_000300: 3.63e-1

DP
type: SiteQuality
SIO_000300: 1.818543e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
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ClippingRankSum
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FS
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SIO_000300: 6.806e0

MQRankSum
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SIO_000300: 2.23e0

InbreedingCoeff
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DP
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QD
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SIO_000300: 1.356e1

MQ
type: SiteQuality
SIO_000300: 5.82e1

BaseQRankSum
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SIO_000300: -7.68e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.611687812379854e-4
allele num: 10404
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

QD
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VQSLOD
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SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.984e0

FS
type: SiteQuality
SIO_000300: 3.449e0

DP
type: SiteQuality
SIO_000300: 1.825384e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

GenotypeDepth
all individuals: 5607
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 233
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11097
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4001
bin: 7.25e1
variant carriers: 0

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