1-161599643-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599643
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599643
    reference: chr 1
allele count: 8057
allele frequency: 7.991311420126559e-2
allele num: 100822
alternate allele: C
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.352A>G
  hgvsp: ENSP00000433642.1:p.Asn118Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.244A>G
  hgvsp: ENSP00000294800.3:p.Asn82Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.305A>G
  hgvsp: ENSP00000394204.2:p.Asn103Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.244A>G
  hgvsp: ENSP00000356941.2:p.Asn82Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41539T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+515A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.193A>G
  hgvsp: ENSP00000437084.1:p.Asn65Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.398A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41411T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41411T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41411T>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 8.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 3.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.75e1
  variant carriers: 1580
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 5.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.25e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 6.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 18016
  bin: 2.25e1
  variant carriers: 588
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 9.75e1
  variant carriers: 921
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 7.5e0
  variant carriers: 2955
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 8.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 2.5e0
  variant carriers: 688
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 1.25e1
  variant carriers: 2841
genotype quality: GenotypeQuality
hgvs: p.Asn118Asp
num of homozygotes: 2443
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

1-161599648-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599648
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599648
    reference: chr 1
allele count: 1
allele frequency: 8.61000137760022e-6
allele num: 116144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.188C>T
  hgvsp: ENSP00000437084.1:p.Thr63Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.347C>T
  hgvsp: ENSP00000433642.1:p.Thr116Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.239C>T
  hgvsp: ENSP00000356941.2:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41416G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.239C>T
  hgvsp: ENSP00000294800.3:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.300C>T
  hgvsp: ENSP00000394204.2:p.Thr101Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+510C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41534G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.393C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41416G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41416G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr116Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

1-161599654-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599654
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599654
    reference: chr 1
allele count: 4989
allele frequency: 4.208350906790384e-2
allele num: 118550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.233C>A
  hgvsp: ENSP00000356941.2:p.Ala78Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41422G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41422G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41422G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.387C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.341C>A
  hgvsp: ENSP00000433642.1:p.Ala114Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41528G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.294C>A
  hgvsp: ENSP00000394204.2:p.Ala99Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.233C>A
  hgvsp: ENSP00000294800.3:p.Ala78Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.182C>A
  hgvsp: ENSP00000437084.1:p.Ala61Asp
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+504C>A
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 22732
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 4924
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 8.75e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 9.75e1
  variant carriers: 3415
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 7.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 8.25e1
  variant carriers: 112
genotype quality: GenotypeQuality
hgvs: p.Ala114Asp
num of homozygotes: 479
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-161599655-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599655
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599655
    reference: chr 1
allele count: 1
allele frequency: 8.407317729351627e-6
allele num: 118944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.293G>T
  hgvsp: ENSP00000394204.2:p.Ala99Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41423C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41527C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.340G>T
  hgvsp: ENSP00000433642.1:p.Ala114Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.232G>T
  hgvsp: ENSP00000294800.3:p.Ala78Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.181G>T
  hgvsp: ENSP00000437084.1:p.Ala61Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.232G>T
  hgvsp: ENSP00000356941.2:p.Ala78Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41423C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41423C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.386G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+503G>T
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala114Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-161599655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599655
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599655
    reference: chr 1
allele count: 78
allele frequency: 6.55770782889427e-4
allele num: 118944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+503G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.293G>A
  hgvsp: ENSP00000394204.2:p.Ala99Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41423C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.232G>A
  hgvsp: ENSP00000356941.2:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.181G>A
  hgvsp: ENSP00000437084.1:p.Ala61Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.340G>A
  hgvsp: ENSP00000433642.1:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41423C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41527C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.232G>A
  hgvsp: ENSP00000294800.3:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41423C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.386G>A
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 9.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala114Thr
num of homozygotes: 10
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

1-161599656-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599656
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599656
    reference: chr 1
allele count: 7
allele frequency: 5.872581754727428e-5
allele num: 119198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.231C>T
  hgvsp: ENST00000294800.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.292C>T
  hgvsp: ENST00000421702.2:c.292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41424G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+502C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41526G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41424G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.180C>T
  hgvsp: ENST00000534776.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41424G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.339C>T
  hgvsp: ENST00000531221.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.231C>T
  hgvsp: ENST00000367964.2:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.385C>T
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp113Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-161599660-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599660
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599660
    reference: chr 1
allele count: 2
allele frequency: 1.668112364048842e-5
allele num: 119896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+498T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41522A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.381T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41428A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.335T>C
  hgvsp: ENSP00000433642.1:p.Ile112Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.227T>C
  hgvsp: ENSP00000294800.3:p.Ile76Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.176T>C
  hgvsp: ENSP00000437084.1:p.Ile59Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41428A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.288T>C
  hgvsp: ENSP00000394204.2:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41428A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.227T>C
  hgvsp: ENSP00000356941.2:p.Ile76Thr
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile112Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

1-161599671-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599671
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599671
    reference: chr 1
allele count: 3
allele frequency: 2.489461280578883e-5
allele num: 120508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+487G>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41439C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.324G>C
  hgvsp: ENST00000531221.1:c.324G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.165G>C
  hgvsp: ENST00000534776.1:c.165G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.370G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.216G>C
  hgvsp: ENST00000294800.3:c.216G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.216G>C
  hgvsp: ENST00000367964.2:c.216G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.277G>C
  hgvsp: ENST00000421702.2:c.277G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41511C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41439C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41439C>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser108Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

1-161599671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599671
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599671
    reference: chr 1
allele count: 2
allele frequency: 1.659640853719255e-5
allele num: 120508
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.324G>A
  hgvsp: ENST00000531221.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41511C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.216G>A
  hgvsp: ENST00000367964.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.216G>A
  hgvsp: ENST00000294800.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.277G>A
  hgvsp: ENST00000421702.2:c.277G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41439C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41439C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.165G>A
  hgvsp: ENST00000534776.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41439C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+487G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.370G>A
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser108Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

1-161599672-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599672
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599672
    reference: chr 1
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.164C>T
  hgvsp: ENSP00000437084.1:p.Ser55Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.369C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.215C>T
  hgvsp: ENSP00000356941.2:p.Ser72Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.276C>T
  hgvsp: ENSP00000394204.2:p.Ser93Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41440G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41440G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.215C>T
  hgvsp: ENSP00000294800.3:p.Ser72Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.323C>T
  hgvsp: ENSP00000433642.1:p.Ser108Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+486C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41510G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41440G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser108Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-161599678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599678
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599678
    reference: chr 1
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41446T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+480A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41446T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.363A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.158A>G
  hgvsp: ENSP00000437084.1:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41446T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.270A>G
  hgvsp: ENSP00000394204.2:p.Gln91Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.209A>G
  hgvsp: ENSP00000294800.3:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.317A>G
  hgvsp: ENSP00000433642.1:p.Gln106Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41504T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.209A>G
  hgvsp: ENSP00000356941.2:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln106Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

1-161599679-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599679
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599679
    reference: chr 1
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41447G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.157C>G
  hgvsp: ENSP00000437084.1:p.Gln53Glu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.269C>G
  hgvsp: ENSP00000394204.2:p.Gln91Glu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.362C>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.208C>G
  hgvsp: ENSP00000356941.2:p.Gln70Glu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41503G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.316C>G
  hgvsp: ENSP00000433642.1:p.Gln106Glu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.208C>G
  hgvsp: ENSP00000294800.3:p.Gln70Glu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+479C>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41447G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41447G>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln106Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

1-161599681-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599681
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599681
    reference: chr 1
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41501C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.360G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.206G>A
  hgvsp: ENSP00000294800.3:p.Ser69Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.314G>A
  hgvsp: ENSP00000433642.1:p.Ser105Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41449C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41449C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.206G>A
  hgvsp: ENSP00000356941.2:p.Ser69Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.570G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.267G>A
  hgvsp: ENSP00000394204.2:p.Ser90Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.155G>A
  hgvsp: ENSP00000437084.1:p.Ser52Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41449C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+477G>A
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser105Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-161599685-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599685
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599685
    reference: chr 1
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.566T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.202T>C
  hgvsp: ENSP00000294800.3:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.263T>C
  hgvsp: ENSP00000394204.2:p.Ser89Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.310T>C
  hgvsp: ENSP00000433642.1:p.Ser104Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.151T>C
  hgvsp: ENSP00000437084.1:p.Ser51Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41453A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41497A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41453A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+473T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41453A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.356T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.202T>C
  hgvsp: ENSP00000356941.2:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser104Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

1-161599686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599686
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599686
    reference: chr 1
allele count: 4
allele frequency: 3.320328712542542e-5
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.309C>T
  hgvsp: ENST00000531221.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41454G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.565C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.262C>T
  hgvsp: ENST00000421702.2:c.262C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.201C>T
  hgvsp: ENST00000294800.3:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.150C>T
  hgvsp: ENST00000534776.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.201C>T
  hgvsp: ENST00000367964.2:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41454G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.355C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+472C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41454G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41496G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile103Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

1-161599686-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599686
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599686
    reference: chr 1
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+472C>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.201C>A
  hgvsp: ENST00000294800.3:c.201C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.150C>A
  hgvsp: ENST00000534776.1:c.150C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.309C>A
  hgvsp: ENST00000531221.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41454G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41454G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41496G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.565C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.201C>A
  hgvsp: ENST00000367964.2:c.201C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.355C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.262C>A
  hgvsp: ENST00000421702.2:c.262C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41454G>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile103Ile
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-161599690-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599690
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599690
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 120440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.146T>A
  hgvsp: ENSP00000437084.1:p.Leu49His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.197T>A
  hgvsp: ENSP00000294800.3:p.Leu66His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.197T>A
  hgvsp: ENSP00000356941.2:p.Leu66His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.258T>A
  hgvsp: ENSP00000394204.2:p.Leu87His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41458A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.561T>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.305T>A
  hgvsp: ENSP00000433642.1:p.Leu102His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+468T>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41492A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.351T>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41458A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41458A>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-161599691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599691
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599691
    reference: chr 1
allele count: 4
allele frequency: 3.321100612743063e-5
allele num: 120442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.257C>T
  hgvsp: ENSP00000394204.2:p.Leu87Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41459G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.196C>T
  hgvsp: ENSP00000294800.3:p.Leu66Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41459G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.196C>T
  hgvsp: ENSP00000356941.2:p.Leu66Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+467C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41491G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.350C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.560C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.145C>T
  hgvsp: ENSP00000437084.1:p.Leu49Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.304C>T
  hgvsp: ENSP00000433642.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41459G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102Phe
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-161599693-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599693
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599693
    reference: chr 1
allele count: 70158
allele frequency: 5.887318743286788e-1
allele num: 119168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.255A>G
  hgvsp: ENSP00000394204.2:p.Asn86Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.302A>G
  hgvsp: ENSP00000433642.1:p.Asn101Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41461T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41489T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+465A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.194A>G
  hgvsp: ENSP00000294800.3:p.Asn65Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.194A>G
  hgvsp: ENSP00000356941.2:p.Asn65Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.348A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41461T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.143A>G
  hgvsp: ENSP00000437084.1:p.Asn48Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.558A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41461T>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 1461
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 774
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 372
genotype depth: GenotypeDepth
  all individuals: 17931
  bin: 9.75e1
  variant carriers: 17648
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 2.25e1
  variant carriers: 1099
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 4.75e1
  variant carriers: 2470
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.75e1
  variant carriers: 2148
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 8.25e1
  variant carriers: 2050
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 3.25e1
  variant carriers: 1758
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 7.25e1
  variant carriers: 2098
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 5.25e1
  variant carriers: 2524
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 6.25e1
  variant carriers: 2157
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.25e1
  variant carriers: 2467
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 5.75e1
  variant carriers: 2369
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 6.75e1
  variant carriers: 2095
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 7.75e1
  variant carriers: 2059
genotype quality: GenotypeQuality
hgvs: p.Asn101Ser
num of homozygotes: 21003
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

1-161599695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599695
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599695
    reference: chr 1
allele count: 4
allele frequency: 3.320328712542542e-5
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.346G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.141G>A
  hgvsp: ENST00000534776.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.556G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.253G>A
  hgvsp: ENST00000421702.2:c.253G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41463C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.300G>A
  hgvsp: ENST00000531221.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41463C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.192G>A
  hgvsp: ENST00000367964.2:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.192G>A
  hgvsp: ENST00000294800.3:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41463C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41487C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+463G>A
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15892
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu100Glu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

1-161599696-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599696
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599696
    reference: chr 1
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.140A>G
  hgvsp: ENSP00000437084.1:p.Glu47Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+462A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.299A>G
  hgvsp: ENSP00000433642.1:p.Glu100Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41464T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.191A>G
  hgvsp: ENSP00000294800.3:p.Glu64Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.252A>G
  hgvsp: ENSP00000394204.2:p.Glu85Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41464T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.555A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41486T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.345A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.191A>G
  hgvsp: ENSP00000356941.2:p.Glu64Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41464T>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu100Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-161599699-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599699
    reference: chr 1
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41483T>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.249A>T
  hgvsp: ENSP00000394204.2:p.Asn84Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.188A>T
  hgvsp: ENSP00000294800.3:p.Asn63Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.342A>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41467T>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.296A>T
  hgvsp: ENSP00000433642.1:p.Asn99Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.188A>T
  hgvsp: ENSP00000356941.2:p.Asn63Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.552A>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+459A>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41467T>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.137A>T
  hgvsp: ENSP00000437084.1:p.Asn46Ile
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41467T>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn99Ile
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: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

1-161599699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599699
    reference: chr 1
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.296A>G
  hgvsp: ENSP00000433642.1:p.Asn99Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+459A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.188A>G
  hgvsp: ENSP00000294800.3:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.552A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.137A>G
  hgvsp: ENSP00000437084.1:p.Asn46Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.342A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41467T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.249A>G
  hgvsp: ENSP00000394204.2:p.Asn84Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41467T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41483T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41467T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.188A>G
  hgvsp: ENSP00000356941.2:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn99Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-161599702-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599702
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599702
    reference: chr 1
allele count: 1
allele frequency: 8.299168423323983e-6
allele num: 120494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.339A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.185A>G
  hgvsp: ENSP00000294800.3:p.His62Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41470T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+456A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.134A>G
  hgvsp: ENSP00000437084.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.293A>G
  hgvsp: ENSP00000433642.1:p.His98Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41470T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.246A>G
  hgvsp: ENSP00000394204.2:p.His83Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41480T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.185A>G
  hgvsp: ENSP00000356941.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.549A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41470T>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His98Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

1-161599707-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599707
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599707
    reference: chr 1
allele count: 2
allele frequency: 1.65953068472236e-5
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.544G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.241G>A
  hgvsp: ENSP00000394204.2:p.Trp81Ter
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.133+41475C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.288G>A
  hgvsp: ENSP00000433642.1:p.Trp96Ter
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+451G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.334G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.129G>A
  hgvsp: ENSP00000437084.1:p.Trp43Ter
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.180G>A
  hgvsp: ENSP00000356941.2:p.Trp60Ter
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.180G>A
  hgvsp: ENSP00000294800.3:p.Trp60Ter
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.133+41475C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41475C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.133+41475C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp96Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-161599711-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599711
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599711
    reference: chr 1
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41471T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41471T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41471T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+447A>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.330A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.284A>C
  hgvsp: ENSP00000433642.1:p.Gln95Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.176A>C
  hgvsp: ENSP00000294800.3:p.Gln59Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.237A>C
  hgvsp: ENSP00000394204.2:p.Gln80Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.540A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41471T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.176A>C
  hgvsp: ENSP00000356941.2:p.Gln59Pro
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.125A>C
  hgvsp: ENSP00000437084.1:p.Gln42Pro
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln95Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-161599717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599717
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599717
    reference: chr 1
allele count: 2
allele frequency: 1.658814942605003e-5
allele num: 120568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+441C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.324C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41465G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41465G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.231C>T
  hgvsp: ENSP00000394204.2:p.Ser78Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.278C>T
  hgvsp: ENSP00000433642.1:p.Ser93Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.170C>T
  hgvsp: ENSP00000356941.2:p.Ser57Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.534C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.119C>T
  hgvsp: ENSP00000437084.1:p.Ser40Phe
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41465G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41465G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.170C>T
  hgvsp: ENSP00000294800.3:p.Ser57Phe
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser93Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-161599722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599722
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599722
    reference: chr 1
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+436C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41460G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.165C>T
  hgvsp: ENST00000367964.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.226C>T
  hgvsp: ENST00000421702.2:c.226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41460G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41460G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.319C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.165C>T
  hgvsp: ENST00000294800.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41460G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.529C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.114C>T
  hgvsp: ENST00000534776.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.273C>T
  hgvsp: ENST00000531221.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp91Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

1-161599724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599724
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599724
    reference: chr 1
allele count: 2
allele frequency: 1.658017342861406e-5
allele num: 120626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41458C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.112G>A
  hgvsp: ENSP00000437084.1:p.Asp38Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.224G>A
  hgvsp: ENSP00000394204.2:p.Asp76Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41458C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.271G>A
  hgvsp: ENSP00000433642.1:p.Asp91Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41458C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.317G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.163G>A
  hgvsp: ENSP00000294800.3:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41458C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.163G>A
  hgvsp: ENSP00000356941.2:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.527G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+434G>A
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp91Asn
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

1-161599727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599727
    reference: chr 1
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.524G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.221G>A
  hgvsp: ENSP00000394204.2:p.Glu75Lys
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.160G>A
  hgvsp: ENSP00000294800.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.109G>A
  hgvsp: ENSP00000437084.1:p.Glu37Lys
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41455C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41455C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41455C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.314G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+431G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.160G>A
  hgvsp: ENSP00000356941.2:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.268G>A
  hgvsp: ENSP00000433642.1:p.Glu90Lys
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41455C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu90Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

1-161599729-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599729
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599729
    reference: chr 1
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+429C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.158C>T
  hgvsp: ENSP00000356941.2:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.312C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.107C>T
  hgvsp: ENSP00000437084.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.219C>T
  hgvsp: ENSP00000394204.2:p.Pro74Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.266C>T
  hgvsp: ENSP00000433642.1:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41453G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41453G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.522C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.158C>T
  hgvsp: ENSP00000294800.3:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41453G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41453G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro89Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-161599730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599730
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599730
    reference: chr 1
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41452G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.157C>T
  hgvsp: ENSP00000356941.2:p.Pro53Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.157C>T
  hgvsp: ENSP00000294800.3:p.Pro53Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.521C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.265C>T
  hgvsp: ENSP00000433642.1:p.Pro89Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41452G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.106C>T
  hgvsp: ENSP00000437084.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.311C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.218C>T
  hgvsp: ENSP00000394204.2:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+428C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41452G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41452G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro89Ser
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-161599733-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599733
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599733
    reference: chr 1
allele count: 3
allele frequency: 2.4906600249066e-5
allele num: 120450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.215T>A
  hgvsp: ENSP00000394204.2:p.Ser73Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.154T>A
  hgvsp: ENSP00000356941.2:p.Ser52Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41449A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.518T>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.154T>A
  hgvsp: ENSP00000294800.3:p.Ser52Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41449A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.262T>A
  hgvsp: ENSP00000433642.1:p.Ser88Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41449A>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.103T>A
  hgvsp: ENSP00000437084.1:p.Ser35Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.308T>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+425T>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41449A>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser88Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-161599735-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599735
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599735
    reference: chr 1
allele count: 3
allele frequency: 2.490701381509033e-5
allele num: 120448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+423A>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.101A>C
  hgvsp: ENSP00000437084.1:p.Tyr34Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.516A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41447T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.152A>C
  hgvsp: ENSP00000294800.3:p.Tyr51Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.260A>C
  hgvsp: ENSP00000433642.1:p.Tyr87Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.152A>C
  hgvsp: ENSP00000356941.2:p.Tyr51Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.213A>C
  hgvsp: ENSP00000394204.2:p.Tyr72Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41447T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.306A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41447T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41447T>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 24011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Tyr87Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

1-161599736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599736
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599736
    reference: chr 1
allele count: 1
allele frequency: 8.302337938363443e-6
allele num: 120448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41446A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+422T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41446A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41446A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.259T>C
  hgvsp: ENSP00000433642.1:p.Tyr87His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.212T>C
  hgvsp: ENSP00000394204.2:p.Tyr72His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.151T>C
  hgvsp: ENSP00000356941.2:p.Tyr51His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.305T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.151T>C
  hgvsp: ENSP00000294800.3:p.Tyr51His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.515T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.100T>C
  hgvsp: ENSP00000437084.1:p.Tyr34His
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41446A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 24011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr87His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-161599739-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599739
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599739
    reference: chr 1
allele count: 27
allele frequency: 2.242972021000864e-4
allele num: 120376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.302G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+419G>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.148G>T
  hgvsp: ENSP00000356941.2:p.Ala50Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41443C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.97G>T
  hgvsp: ENSP00000437084.1:p.Ala33Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.209G>T
  hgvsp: ENSP00000394204.2:p.Ala71Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.512G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41443C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.256G>T
  hgvsp: ENSP00000433642.1:p.Ala86Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41443C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.148G>T
  hgvsp: ENSP00000294800.3:p.Ala50Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41443C>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala86Ser
num of homozygotes: 2
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

1-161599742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599742
    reference: chr 1
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.145G>A
  hgvsp: ENSP00000356941.2:p.Gly49Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41440C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.94G>A
  hgvsp: ENSP00000437084.1:p.Gly32Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.206G>A
  hgvsp: ENSP00000394204.2:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.299G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41440C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+416G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.253G>A
  hgvsp: ENSP00000433642.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.509G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.145G>A
  hgvsp: ENSP00000294800.3:p.Gly49Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41440C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41440C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly85Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

1-161599749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599749
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599749
    reference: chr 1
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41433C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.246G>A
  hgvsp: ENST00000531221.1:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41433C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.138G>A
  hgvsp: ENST00000294800.3:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41433C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+409G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.502G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41433C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.199G>A
  hgvsp: ENST00000421702.2:c.199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.292G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.138G>A
  hgvsp: ENST00000367964.2:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.87G>A
  hgvsp: ENST00000534776.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys82Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

1-161599754-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599754
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599754
    reference: chr 1
allele count: 1
allele frequency: 8.740953113527499e-6
allele num: 114404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41428G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.133C>T
  hgvsp: ENST00000367964.2:c.133C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.497C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41428G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.194C>T
  hgvsp: ENST00000421702.2:c.194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+404C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.287C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41428G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.241C>T
  hgvsp: ENST00000531221.1:c.241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.82C>T
  hgvsp: ENST00000534776.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41428G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.133C>T
  hgvsp: ENST00000294800.3:c.133C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu81Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-161599754-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599754
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599754
    reference: chr 1
allele count: 11
allele frequency: 9.615048424880249e-5
allele num: 114404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41428G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.497C>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41428G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.82C>G
  hgvsp: ENSP00000437084.1:p.Leu28Val
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.194C>G
  hgvsp: ENSP00000394204.2:p.Leu66Val
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41428G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+404C>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41428G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.133C>G
  hgvsp: ENSP00000294800.3:p.Leu45Val
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.241C>G
  hgvsp: ENSP00000433642.1:p.Leu81Val
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.287C>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.133C>G
  hgvsp: ENSP00000356941.2:p.Leu45Val
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu81Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-161599755-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599755
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599755
    reference: chr 1
allele count: 2
allele frequency: 1.748068384435199e-5
allele num: 114412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41427A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.496T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.81T>C
  hgvsp: ENST00000534776.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.193T>C
  hgvsp: ENST00000421702.2:c.193T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.240T>C
  hgvsp: ENST00000531221.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+403T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41427A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.132T>C
  hgvsp: ENST00000367964.2:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.286T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.132T>C
  hgvsp: ENST00000294800.3:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41427A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41427A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr80Thr
num of homozygotes: 1
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

1-161599763-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599763
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599763
    reference: chr 1
allele count: 3
allele frequency: 2.973771336809342e-5
allele num: 100882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+395A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.232A>G
  hgvsp: ENSP00000433642.1:p.Ser78Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.124A>G
  hgvsp: ENSP00000356941.2:p.Ser42Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.124A>G
  hgvsp: ENSP00000294800.3:p.Ser42Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41419T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.185A>G
  hgvsp: ENSP00000394204.2:p.Ser63Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41419T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.73A>G
  hgvsp: ENSP00000437084.1:p.Ser25Gly
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41419T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.488A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.278A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41419T>C
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser78Gly
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-161599773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599773
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599773
    reference: chr 1
allele count: 12
allele frequency: 1.192250372578241e-4
allele num: 100650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.268T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.63T>C
  hgvsp: ENST00000534776.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.114T>C
  hgvsp: ENST00000294800.3:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.114T>C
  hgvsp: ENST00000367964.2:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.478T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.175T>C
  hgvsp: ENST00000421702.2:c.175T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+385T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41409A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41409A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.222T>C
  hgvsp: ENST00000531221.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41409A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41409A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu74Leu
num of homozygotes: 4
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-161599778-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599778
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599778
    reference: chr 1
allele count: 33
allele frequency: 3.281035614150212e-4
allele num: 100578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+380G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.58G>A
  hgvsp: ENSP00000437084.1:p.Val20Met
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.170G>A
  hgvsp: ENSP00000394204.2:p.Val58Met
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41404C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.473G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.263G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41404C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.217G>A
  hgvsp: ENSP00000433642.1:p.Val73Met
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.109G>A
  hgvsp: ENSP00000356941.2:p.Val37Met
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41404C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.109G>A
  hgvsp: ENSP00000294800.3:p.Val37Met
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41404C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22547
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val73Met
num of homozygotes: 12
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

1-161599779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599779
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599779
    reference: chr 1
allele count: 4
allele frequency: 3.978436872152931e-5
allele num: 100542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.108C>T
  hgvsp: ENST00000294800.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.108C>T
  hgvsp: ENST00000367964.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+379C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.472C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41403G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.57C>T
  hgvsp: ENST00000534776.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.216C>T
  hgvsp: ENST00000531221.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.169C>T
  hgvsp: ENST00000421702.2:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.262C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41403G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41403G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41403G>A
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser72Ser
num of homozygotes: 1
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

1-161599779-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599779
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599779
    reference: chr 1
allele count: 11
allele frequency: 1.094070139842056e-4
allele num: 100542
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.169C>G
  hgvsp: ENSP00000394204.2:p.Ser57Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+379C>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.216C>G
  hgvsp: ENSP00000433642.1:p.Ser72Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41403G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.108C>G
  hgvsp: ENSP00000294800.3:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.262C>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41403G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.57C>G
  hgvsp: ENSP00000437084.1:p.Ser19Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41403G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41403G>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.108C>G
  hgvsp: ENSP00000356941.2:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.472C>G
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 22540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser72Arg
num of homozygotes: 4
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-161599794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599794
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599794
    reference: chr 1
allele count: 18
allele frequency: 1.806394637015033e-4
allele num: 99646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.93G>A
  hgvsp: ENST00000367964.2:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41388C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.201G>A
  hgvsp: ENST00000531221.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41388C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.42G>A
  hgvsp: ENST00000534776.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.457G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.93G>A
  hgvsp: ENST00000294800.3:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.154G>A
  hgvsp: ENST00000421702.2:c.154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+364G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41388C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.247G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41388C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Glu67Glu
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-161599808-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599808
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599808
    reference: chr 1
allele count: 11
allele frequency: 1.136269729774399e-4
allele num: 96808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.28G>C
  hgvsp: ENSP00000437084.1:p.Val10Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.443G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.79G>C
  hgvsp: ENSP00000356941.2:p.Val27Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41374C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.187G>C
  hgvsp: ENSP00000433642.1:p.Val63Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.233G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.140G>C
  hgvsp: ENSP00000394204.2:p.Val48Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41374C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.79G>C
  hgvsp: ENSP00000294800.3:p.Val27Leu
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41374C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41374C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+350G>C
  variant of: http://identifiers.org/hgnc/3619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14074
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val63Leu
num of homozygotes: 2
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-161599811-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599811
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599811
    reference: chr 1
allele count: 1
allele frequency: 1.043797753747234e-5
allele num: 95804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41371C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.230G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.184G>T
  hgvsp: ENSP00000433642.1:p.Ala62Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.137G>T
  hgvsp: ENSP00000394204.2:p.Ala47Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41371C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41371C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+347G>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41371C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.25G>T
  hgvsp: ENSP00000437084.1:p.Ala9Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.76G>T
  hgvsp: ENSP00000356941.2:p.Ala26Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.76G>T
  hgvsp: ENSP00000294800.3:p.Ala26Ser
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.440G>T
  variant of: http://identifiers.org/hgnc/3620
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala62Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-161599811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599811
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599811
    reference: chr 1
allele count: 3
allele frequency: 3.131393261241702e-5
allele num: 95804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.76G>A
  hgvsp: ENSP00000356941.2:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.137G>A
  hgvsp: ENSP00000394204.2:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.76G>A
  hgvsp: ENSP00000294800.3:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.440G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41371C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.230G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41371C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.25G>A
  hgvsp: ENSP00000437084.1:p.Ala9Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+347G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41371C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.184G>A
  hgvsp: ENSP00000433642.1:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41371C>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18889
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala62Thr
num of homozygotes: 1
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

1-161599831-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599831
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599831
    reference: chr 1
allele count: 35
allele frequency: 4.343078373951457e-4
allele num: 80588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.62-6C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+327C>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.170-6C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.11-6C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41351G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41351G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.126-9C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.420C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.62-6C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.210C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41351G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41351G>T
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.170-6C>A
num of homozygotes: 2
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

1-161599842-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599842
    reference: chr 1
allele count: 1
allele frequency: 1.512950859356088e-5
allele num: 66096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41340A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41340A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+316T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.126-20T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.62-17T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41340A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.170-17T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.409T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.11-17T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.199T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.62-17T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41340A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-161599860-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599860
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599860
    reference: chr 1
allele count: 2
allele frequency: 3.771450122572129e-5
allele num: 53030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.62-35C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.170-35C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.11-35C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.126-38C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+298C>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.391C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.181C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41322G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.62-35C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41322G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41322G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41322G>T
  variant of: http://identifiers.org/hgnc/3618
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15919
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

1-161599870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599870
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599870
    reference: chr 1
allele count: 6
allele frequency: 1.244142163977937e-4
allele num: 48226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41312G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.381C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.11-45C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.62-45C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41312G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.126-48C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41312G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.62-45C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+288C>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41312G>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.171C>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.170-45C>T
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

1-161599872-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161599872
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161599872
    reference: chr 1
allele count: 1
allele frequency: 2.164408467165924e-5
allele num: 46202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.62-47G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41310C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.379G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41310C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.170-47G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41310C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41310C>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000533780
  gene symbol: FCGR3B
  hgvsc: ENST00000533780.1:n.169G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.126-50G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.62-47G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.11-47G>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+286G>C
  variant of: http://identifiers.org/hgnc/3619
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21406
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-161600109-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600109
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600109
    reference: chr 1
allele count: 2
allele frequency: 1.753678340318819e-5
allele num: 114046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41073C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41073C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+49G>T
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41073C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.142G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+49G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41073C>A
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+49G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+49G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+49G>T
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+49G>T
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12467
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

1-161600109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600109
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600109
    reference: chr 1
allele count: 12668
allele frequency: 1.11077986075794e-1
allele num: 114046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41073C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.142G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41073C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41073C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+49G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41073C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+49G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+49G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+49G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+49G>A
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+49G>A
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 1.75e1
  variant carriers: 1222
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 12467
  bin: 2.25e1
  variant carriers: 1708
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 7.5e0
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 2.75e1
  variant carriers: 1696
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 1.25e1
  variant carriers: 674
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.75e1
  variant carriers: 542
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.25e1
  variant carriers: 719
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 3.25e1
  variant carriers: 1291
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.75e1
  variant carriers: 1017
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 9.75e1
  variant carriers: 1134
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.75e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.25e1
  variant carriers: 374
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 7.75e1
  variant carriers: 70
num of homozygotes: 767
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-161600113-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600113
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600113
    reference: chr 1
allele count: 1
allele frequency: 8.767469182345825e-6
allele num: 114058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41069A>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.138T>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+45T>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41069A>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+45T>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41069A>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+45T>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41069A>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+45T>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+45T>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+45T>G
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

1-161600114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600114
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600114
    reference: chr 1
allele count: 4
allele frequency: 3.507787287778869e-5
allele num: 114032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41068T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.137A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+44A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+44A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41068T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+44A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41068T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41068T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+44A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+44A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+44A>G
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17078
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5456
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-161600115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600115
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600115
    reference: chr 1
allele count: 1
allele frequency: 8.769775844529415e-6
allele num: 114028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+43T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.136T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+43T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41067A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41067A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41067A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+43T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+43T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41067A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+43T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+43T>C
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

1-161600116-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600116
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600116
    reference: chr 1
allele count: 626
allele frequency: 5.492866293455943e-3
allele num: 113966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41066T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41066T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+42A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+42A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+42A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.135A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41066T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41066T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+42A>G
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+42A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+42A>G
  variant of: http://identifiers.org/hgnc/3620
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 5493
  bin: 3.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 1.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 14167
  bin: 2.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 17043
  bin: 2.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 5
num of homozygotes: 53
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

1-161600117-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600117
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600117
    reference: chr 1
allele count: 1
allele frequency: 8.779939594015594e-6
allele num: 113896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41065G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+41C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.134C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+41C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+41C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41065G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41065G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+41C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41065G>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+41C>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+41C>A
  variant of: http://identifiers.org/hgnc/3619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

1-161600126-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600126
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600126
    reference: chr 1
allele count: 1
allele frequency: 8.796622097114708e-6
allele num: 113680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+32A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41056T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+32A>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41056T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+32A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+32A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.125A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+32A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+32A>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41056T>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41056T>G
  variant of: http://identifiers.org/hgnc/3618
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum

1-161600134-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600134
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600134
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 113472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41048T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+24A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.117A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+24A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41048T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+24A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+24A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+24A>G
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41048T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41048T>C
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+24A>G
  variant of: http://identifiers.org/hgnc/3619
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-161600147-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600147
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600147
    reference: chr 1
allele count: 4
allele frequency: 3.547860640034059e-5
allele num: 112744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41035A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41035A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+11T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+11T>C
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41035A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+11T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.104T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+11T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+11T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+11T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41035A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17711
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-161600149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600149
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600149
    reference: chr 1
allele count: 2
allele frequency: 1.77679856434676e-5
allele num: 112562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.61+9G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41033C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.102G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41033C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.10+9G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.125+9G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.61+9G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.169+9G>A
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41033C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41033C>T
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.61+9G>A
  variant of: http://identifiers.org/hgnc/3619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16915
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

1-161600159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600159
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 161600159
    reference: chr 1
allele count: 1
allele frequency: 8.962179602079226e-6
allele num: 111580
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000356941
  ensembl transcript: ENST00000367964
  gene symbol: FCGR3B
  hgvsc: ENST00000367964.2:c.60T>C
  hgvsp: ENST00000367964.2:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162747
  ensembl transcript: ENST00000534489
  gene symbol: FCGR3B
  hgvsc: ENST00000534489.1:n.92T>C
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000433642
  ensembl transcript: ENST00000531221
  gene symbol: FCGR3B
  hgvsc: ENST00000531221.1:c.168T>C
  hgvsp: ENST00000531221.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000294800
  ensembl transcript: ENST00000294800
  gene symbol: FCGR3B
  hgvsc: ENST00000294800.3:c.60T>C
  hgvsp: ENST00000294800.3:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000394204
  ensembl transcript: ENST00000421702
  gene symbol: FCGR3B
  hgvsc: ENST00000421702.2:c.124T>C
  hgvsp: ENST00000421702.2:c.124T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203747
  ensembl protein: ENSP00000444971
  ensembl transcript: ENST00000540048
  gene symbol: FCGR3A
  hgvsc: ENST00000540048.1:c.60T>C
  hgvsp: ENST00000540048.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000404329
  ensembl transcript: ENST00000428605
  gene symbol: FCGR2B
  hgvsc: ENST00000428605.2:c.134-41023A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162747
  ensembl protein: ENSP00000437084
  ensembl transcript: ENST00000534776
  gene symbol: FCGR3B
  hgvsc: ENST00000534776.1:c.9T>C
  hgvsp: ENST00000534776.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3620
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356937
  ensembl transcript: ENST00000367960
  gene symbol: FCGR2B
  hgvsc: ENST00000367960.5:c.113-41023A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000356939
  ensembl transcript: ENST00000367962
  gene symbol: FCGR2B
  hgvsc: ENST00000367962.4:c.134-41023A>G
  variant of: http://identifiers.org/hgnc/3618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072694
  ensembl protein: ENSP00000386038
  ensembl transcript: ENST00000403078
  gene symbol: FCGR2B
  hgvsc: ENST00000403078.3:c.134-41023A>G
  variant of: http://identifiers.org/hgnc/3618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.168T>C
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

1-161600163-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 161600163
allele count: 5
allele frequency: 4.512635379061372e-5
allele num: 110800
alternate allele: T
canonical: true
consequence: missense
filter: PASS
hgvs: p.Arg55Gln
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 1076
bin: 5.75e1
variant carriers: 39

GenotypeDepth
all individuals: 852
bin: 6.75e1
variant carriers: 62

GenotypeDepth
all individuals: 7697
bin: 2.75e1
variant carriers: 258

GenotypeQuality
all individuals: 1301
bin: 8.75e1
variant carriers: 107

GenotypeQuality
all individuals: 1604
bin: 2.25e1
variant carriers: 1122

GenotypeQuality
all individuals: 892
bin: 4.25e1
variant carriers: 423

GenotypeQuality
all individuals: 1189
bin: 3.75e1
variant carriers: 688

GenotypeQuality
all individuals: 1543
bin: 1.75e1
variant carriers: 1134

GenotypeQuality
all individuals: 2955
bin: 2.5e0
variant carriers: 529

GenotypeQuality
all individuals: 1284
bin: 7.5e0
variant carriers: 826

GenotypeQuality
all individuals: 1357
bin: 1.25e1
variant carriers: 968

GenotypeQuality
all individuals: 1144
bin: 2.75e1
variant carriers: 669

GenotypeQuality
all individuals: 967
bin: 5.25e1
variant carriers: 388

GenotypeQuality
all individuals: 2201
bin: 7.25e1
variant carriers: 145

GenotypeQuality
all individuals: 17575
bin: 6.25e1
variant carriers: 243

GenotypeQuality
all individuals: 2397
bin: 8.25e1
variant carriers: 144

GenotypeQuality
all individuals: 999
bin: 4.75e1
variant carriers: 492

GenotypeQuality
all individuals: 1307
bin: 3.25e1
variant carriers: 848

GenotypeQuality
all individuals: 1659
bin: 9.25e1
variant carriers: 100

GenotypeQuality
all individuals: 734
bin: 5.75e1
variant carriers: 267

GenotypeQuality
all individuals: 4692
bin: 6.75e1
variant carriers: 193

GenotypeQuality
all individuals: 2878
bin: 7.75e1
variant carriers: 147

GenotypeQuality
all individuals: 10511
bin: 9.75e1
variant carriers: 1268

African
type: Population
allele count: 841
allele frequency: 1.057861635220126e-1
allele num: 7950
num of homozygotes: 290

Other
type: Population
allele count: 51
allele frequency: 6.710526315789474e-2
allele num: 760
num of homozygotes: 21

Latino
type: Population
allele count: 1170
allele frequency: 1.34297520661157e-1
allele num: 8712
num of homozygotes: 251

South Asian
type: Population
allele count: 1554
allele frequency: 1.169828364950316e-1
allele num: 13284
num of homozygotes: 658

East Asian
type: Population
allele count: 1400
allele frequency: 2.263906856403622e-1
allele num: 6184
num of homozygotes: 477

European (Non-Finnish)
type: Population
allele count: 2874
allele frequency: 4.934244411633417e-2
allele num: 58246
num of homozygotes: 711

European (Finnish)
type: Population
allele count: 167
allele frequency: 2.93703833978192e-2
allele num: 5686
num of homozygotes: 35

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.456e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 8.5657e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.795e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.862e1

MQ
type: SiteQuality
SIO_000300: 2.629e1

MQRankSum
type: SiteQuality
SIO_000300: -3.006e0

DP
type: SiteQuality
SIO_000300: 2.374798e6

QD
type: SiteQuality
SIO_000300: 8.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22407
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18914
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.409434687860531e-5
allele num: 15602
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.773e0

VQSLOD
type: SiteQuality
SIO_000300: -1.282e1

QD
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.129e0

DP
type: SiteQuality
SIO_000300: 2.422663e6

FS
type: SiteQuality
SIO_000300: 2.594e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.543e0

MQ
type: SiteQuality
SIO_000300: 3.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e0

GenotypeQuality
all individuals: 2038
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 953
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2061
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 2600
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 22558
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 21648
bin: 9.75e1
variant carriers: 4382

GenotypeQuality
all individuals: 5567
bin: 6.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1428
bin: 9.25e1
variant carriers: 12

European (Non-Finnish)
type: Population
allele count: 1483
allele frequency: 2.249969656511713e-2
allele num: 65912
num of homozygotes: 13

Other
type: Population
allele count: 25
allele frequency: 2.853881278538813e-2
allele num: 876
num of homozygotes: 3

African
type: Population
allele count: 1874
allele frequency: 1.98685326547922e-1
allele num: 9432
num of homozygotes: 384

European (Finnish)
type: Population
allele count: 192
allele frequency: 2.967542503863988e-2
allele num: 6470
num of homozygotes: 0

Latino
type: Population
allele count: 191
allele frequency: 1.683115967571378e-2
allele num: 11348
num of homozygotes: 7

South Asian
type: Population
allele count: 1223
allele frequency: 7.62278733482922e-2
allele num: 16044
num of homozygotes: 72

East Asian
type: Population
allele count: 1
allele frequency: 1.180916391119509e-4
allele num: 8468
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.91026e6

MQ
type: SiteQuality
SIO_000300: 3.298e1

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.549e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.28e1

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.154e0

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

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

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21127
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2685
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variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5700
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.04777870913663e-4
allele num: 9544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.298e1

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

QD
type: SiteQuality
SIO_000300: 1.463e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.738e-1

DP
type: SiteQuality
SIO_000300: 2.682015e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21127
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1041
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5700
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22942
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 68
allele frequency: 7.124895222129086e-3
allele num: 9544
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.139273811611998e-4
allele num: 11402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.543114153314959e-5
allele num: 66034
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

DP
type: SiteQuality
SIO_000300: 2.682015e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.738e-1

MQ
type: SiteQuality
SIO_000300: 3.298e1

QD
type: SiteQuality
SIO_000300: 1.463e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21112
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2070
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 749
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variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23075
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2689
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.058841325064287e-4
allele num: 66110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 2.681461e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

MQ
type: SiteQuality
SIO_000300: 3.285e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.662e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 23471
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 2692
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variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1493
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21111
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 2
allele frequency: 2.332089552238806e-4
allele num: 8576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

MQRankSum
type: SiteQuality
SIO_000300: -1.374e0

DP
type: SiteQuality
SIO_000300: 2.68649e6

MQ
type: SiteQuality
SIO_000300: 3.139e1

VQSLOD
type: SiteQuality
SIO_000300: -8.053000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.831e0

FS
type: SiteQuality
SIO_000300: 1.8838e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.77e0

QD
type: SiteQuality
SIO_000300: 2.99e0

GenotypeQuality
all individuals: 23595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 2077
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 21115
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5751
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.518e0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

MQ
type: SiteQuality
SIO_000300: 3.161e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 1.0774e1

DP
type: SiteQuality
SIO_000300: 2.691113e6

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

GenotypeQuality
all individuals: 21115
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 1494
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 1047
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variant carriers: 0

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

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

GenotypeQuality
all individuals: 2695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0774e1

DP
type: SiteQuality
SIO_000300: 2.691113e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 3.161e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

GenotypeQuality
all individuals: 23653
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1494
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GenotypeQuality
all individuals: 237
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 2696
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 8.75e1
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GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

QD
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SIO_000300: 1.865e1

ClippingRankSum
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SIO_000300: -1.7e-2

MQRankSum
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SIO_000300: -2.0e-3

MQ
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SIO_000300: 3.13e1

VQSLOD
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SIO_000300: -3.711e0

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

BaseQRankSum
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SIO_000300: -1.979e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

DP
type: SiteQuality
SIO_000300: 2.691406e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
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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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num of homozygotes: 0

MQRankSum
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SIO_000300: -6.4e-2

VQSLOD
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FS
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SIO_000300: 8.85e-1

DP
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BaseQRankSum
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SIO_000300: -2.693e0

ReadPosRankSum
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SIO_000300: 5.46e-1

QD
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SIO_000300: 1.042e1

ClippingRankSum
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SIO_000300: 1.26e0

InbreedingCoeff
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SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 2.417e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.37e-1

VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 2.962e1

QD
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SIO_000300: 5.52e0

DP
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SIO_000300: 2.68654e6

InbreedingCoeff
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SIO_000300: 1.1e-2

MQRankSum
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SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 2.7509e1

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
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

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

Other
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allele 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: 9924
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.214e0

MQ
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SIO_000300: 3.296e1

DP
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SIO_000300: 2.685174e6

FS
type: SiteQuality
SIO_000300: 4.5981e1

VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 1.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ReadPosRankSum
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SIO_000300: 7.099999999999999e-2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

South Asian
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allele frequency: 6.101281269066504e-5
allele num: 16390
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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Latino
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allele frequency: 1.734304543877905e-4
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.006614552014432e-5
allele num: 66520
num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

Other
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East Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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num of homozygotes: 0

MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

African
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allele count: 0
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Latino
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East Asian
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Other
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South Asian
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European (Finnish)
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 3.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

FS
type: SiteQuality
SIO_000300: 1.2562e1

VQSLOD
type: SiteQuality
SIO_000300: -4.355e0

QD
type: SiteQuality
SIO_000300: 1.455e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2690
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
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GenotypeQuality
all individuals: 21127
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.34e0

FS
type: SiteQuality
SIO_000300: 4.0939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.684024e6

VQSLOD
type: SiteQuality
SIO_000300: -1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQ
type: SiteQuality
SIO_000300: 2.86e1

GenotypeDepth
all individuals: 1974
bin: 9.25e1
variant carriers: 1965

GenotypeDepth
all individuals: 2090
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variant carriers: 2081

GenotypeQuality
all individuals: 246
bin: 2.25e1
variant carriers: 172

GenotypeQuality
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bin: 5.25e1
variant carriers: 407

GenotypeQuality
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variant carriers: 544

GenotypeQuality
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bin: 3.75e1
variant carriers: 296

GenotypeQuality
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bin: 2.75e1
variant carriers: 171

GenotypeQuality
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bin: 2.5e0
variant carriers: 105

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 414

GenotypeQuality
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GenotypeQuality
all individuals: 706
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variant carriers: 646

GenotypeQuality
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bin: 1.25e1
variant carriers: 124

GenotypeQuality
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GenotypeQuality
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variant carriers: 657

GenotypeQuality
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bin: 7.5e0
variant carriers: 126

GenotypeQuality
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variant carriers: 342

GenotypeQuality
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variant carriers: 138

GenotypeQuality
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variant carriers: 43198

GenotypeQuality
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bin: 3.25e1
variant carriers: 216

GenotypeQuality
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variant carriers: 596

GenotypeQuality
all individuals: 381
bin: 4.75e1
variant carriers: 363

GenotypeQuality
all individuals: 499
bin: 8.75e1
variant carriers: 481

Latino
type: Population
allele count: 4878
allele frequency: 4.302346092785324e-1
allele num: 11338
num of homozygotes: 689

European (Non-Finnish)
type: Population
allele count: 42904
allele frequency: 6.511853808092767e-1
allele num: 65886
num of homozygotes: 13841

South Asian
type: Population
allele count: 9287
allele frequency: 5.695449527781185e-1
allele num: 16306
num of homozygotes: 2838

Other
type: Population
allele count: 551
allele frequency: 6.191011235955056e-1
allele num: 890
num of homozygotes: 186

African
type: Population
allele count: 5574
allele frequency: 5.695892090741876e-1
allele num: 9786
num of homozygotes: 1869

East Asian
type: Population
allele count: 2987
allele frequency: 3.521575100212214e-1
allele num: 8482
num of homozygotes: 396

European (Finnish)
type: Population
allele count: 3977
allele frequency: 6.137345679012346e-1
allele num: 6480
num of homozygotes: 1184

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e0

MQ
type: SiteQuality
SIO_000300: 2.879e1

FS
type: SiteQuality
SIO_000300: 1.15911e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.870999999999999e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

QD
type: SiteQuality
SIO_000300: 1.337e1

DP
type: SiteQuality
SIO_000300: 4.48982e6

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 1645
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variant carriers: 0

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 192
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 9456
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 266
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GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 366
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GenotypeQuality
all individuals: 344
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GenotypeQuality
all individuals: 1359
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GenotypeQuality
all individuals: 43858
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 4.014452027298274e-4
allele num: 9964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
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SIO_000300: -2.824e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.249e1

FS
type: SiteQuality
SIO_000300: 1.4954e1

VQSLOD
type: SiteQuality
SIO_000300: -6.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 2.871e1

DP
type: SiteQuality
SIO_000300: 1.710919e6

GenotypeDepth
all individuals: 44
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variant carriers: 0

GenotypeDepth
all individuals: 337
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variant carriers: 1

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 259
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variant carriers: 0

GenotypeQuality
all individuals: 180
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GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 379
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GenotypeQuality
all individuals: 1642
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variant carriers: 0

GenotypeQuality
all individuals: 297
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GenotypeQuality
all individuals: 9453
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43828
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GenotypeQuality
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GenotypeQuality
all individuals: 1356
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GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 378
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GenotypeQuality
all individuals: 1075
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GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 96
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.003814495081309e-4
allele num: 9962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
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VQSLOD
type: SiteQuality
SIO_000300: -5.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 3.005e1

QD
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SIO_000300: 8.08e0

ReadPosRankSum
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SIO_000300: -4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 4.05e0

DP
type: SiteQuality
SIO_000300: 1.710739e6

GenotypeDepth
all individuals: 161
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variant carriers: 0

GenotypeDepth
all individuals: 44
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variant carriers: 1

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1633
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 116
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 177
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 179
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GenotypeQuality
all individuals: 1072
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variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 2.933e1

MQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

DP
type: SiteQuality
SIO_000300: 1.711577e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

GenotypeDepth
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variant carriers: 1

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: 548
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

South Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

InbreedingCoeff
type: SiteQuality
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-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
all individuals: 141
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 97
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GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.85e0

MQ
type: SiteQuality
SIO_000300: 3.365e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
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SIO_000300: 8.120000000000001e-1

FS
type: SiteQuality
SIO_000300: 4.3555e1

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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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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num of homozygotes: 0

African
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European (Non-Finnish)
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East Asian
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Latino
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Other
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South Asian
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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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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East Asian
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European (Finnish)
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African
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South Asian
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Latino
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Other
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQ
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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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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Latino
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East Asian
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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MQ
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DP
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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Latino
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African
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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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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African
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Other
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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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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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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DP
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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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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African
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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GenotypeDepth
all individuals: 119
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variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 533
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

FS
type: SiteQuality
SIO_000300: 2.1029e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 3.656e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.719302e6

VQSLOD
type: SiteQuality
SIO_000300: -5.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

QD
type: SiteQuality
SIO_000300: 2.964e1

GenotypeDepth
all individuals: 321
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variant carriers: 0

GenotypeDepth
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 127
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.51304269338388e-5
allele num: 66474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9910
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.135e1

FS
type: SiteQuality
SIO_000300: 3.7325e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.417e0

MQRankSum
type: SiteQuality
SIO_000300: -4.047e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 6.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 3.451e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e0

DP
type: SiteQuality
SIO_000300: 1.716872e6

GenotypeDepth
all individuals: 160
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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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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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1628
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.478664192949907e-4
allele num: 8624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.256e0

VQSLOD
type: SiteQuality
SIO_000300: -9.018000000000001e0

FS
type: SiteQuality
SIO_000300: 1.609e1

MQRankSum
type: SiteQuality
SIO_000300: -6.373e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.033e0

QD
type: SiteQuality
SIO_000300: 5.22e0

MQ
type: SiteQuality
SIO_000300: 3.686e1

DP
type: SiteQuality
SIO_000300: 1.715742e6

GenotypeDepth
all individuals: 277
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 175
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1334
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.714672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

MQ
type: SiteQuality
SIO_000300: 2.724e1

FS
type: SiteQuality
SIO_000300: 1.156e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

VQSLOD
type: SiteQuality
SIO_000300: -5.137e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 44349
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9380
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1616
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1043
bin: 9.75e1
variant carriers: 24

African
type: Population
allele count: 25
allele frequency: 2.525252525252525e-3
allele num: 9900
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.667e0

MQ
type: SiteQuality
SIO_000300: 3.511e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.38e-2

DP
type: SiteQuality
SIO_000300: 1.710378e6

BaseQRankSum
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SIO_000300: -3.293e0

VQSLOD
type: SiteQuality
SIO_000300: -5.088e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.835e0

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

FS
type: SiteQuality
SIO_000300: 1.3205e1

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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variant carriers: 0

GenotypeQuality
all individuals: 175
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 529
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GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66424
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011531458628363e-4
allele num: 9886
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.70725e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

FS
type: SiteQuality
SIO_000300: 1.4403e1

QD
type: SiteQuality
SIO_000300: 6.67e0

MQ
type: SiteQuality
SIO_000300: 3.125e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeDepth
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variant carriers: 1

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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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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variant carriers: 0

GenotypeQuality
all individuals: 527
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66180
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 3.043e0

MQ
type: SiteQuality
SIO_000300: 3.678e1

QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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SIO_000300: 5.67e0

ClippingRankSum
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SIO_000300: 7.33e0

MQRankSum
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SIO_000300: 5.72e0

DP
type: SiteQuality
SIO_000300: 1.706366e6

BaseQRankSum
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SIO_000300: -6.097e0

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

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

South Asian
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allele frequency: 6.496037417175523e-5
allele num: 15394
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64286
num of homozygotes: 0

East Asian
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num of homozygotes: 0

DP
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SIO_000300: 1.710382e6

FS
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 4.26e0

ReadPosRankSum
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SIO_000300: 3.51e0

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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allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

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

Other
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allele frequency: 1.16822429906542e-3
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

European (Non-Finnish)
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allele count: 10
allele frequency: 1.555548642006035e-4
allele num: 64286
num of homozygotes: 0

MQ
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SIO_000300: 4.246e1

VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 1.898e1

ClippingRankSum
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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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allele count: 2
allele frequency: 2.199736031676199e-4
allele num: 9092
num of homozygotes: 1

Other
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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: 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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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 frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 4.06e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.2e-3

MQRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 37970
bin: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13010
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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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: 3
allele frequency: 5.077860528097495e-5
allele num: 59080
num of homozygotes: 1

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

InbreedingCoeff
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SIO_000300: 3.2e-3

FS
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SIO_000300: 1.3427e1

DP
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SIO_000300: 1.5043e6

MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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SIO_000300: 3.29e0

ReadPosRankSum
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SIO_000300: 3.76e0

BaseQRankSum
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SIO_000300: 9.49e-1

QD
type: SiteQuality
SIO_000300: 1.72e1

GenotypeDepth
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variant carriers: 5

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: 1

European (Non-Finnish)
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allele count: 7
allele frequency: 1.186601573094657e-4
allele num: 58992
num of homozygotes: 3

African
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allele num: 8106
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Other
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European (Finnish)
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allele frequency: 0.0e0
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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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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.2671e1

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

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5372
num of homozygotes: 0

Other
type: Population
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 58970
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African
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allele frequency: 8.64410965670536e-4
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South Asian
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FS
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BaseQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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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
type: Population
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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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African
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 3

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
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GenotypeQuality
all individuals: 958
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 7.710100231303007e-4
allele num: 12970
num of homozygotes: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58958
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.864280387770321e-4
allele num: 5364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e0

QD
type: SiteQuality
SIO_000300: 6.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

DP
type: SiteQuality
SIO_000300: 1.488947e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQ
type: SiteQuality
SIO_000300: 3.392e1

FS
type: SiteQuality
SIO_000300: 6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.111e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.49e-2

GenotypeDepth
all individuals: 21
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.074400491904078e-4
allele num: 58548
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12882
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5270
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.223e-1

FS
type: SiteQuality
SIO_000300: 6.25e-1

QD
type: SiteQuality
SIO_000300: 1.725e1

ReadPosRankSum
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SIO_000300: 4.47e-1

BaseQRankSum
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SIO_000300: -4.502e0

MQ
type: SiteQuality
SIO_000300: 4.326e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.01e-1

DP
type: SiteQuality
SIO_000300: 1.477006e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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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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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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 152
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.924759405074366e-4
allele num: 57150
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5420
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.193e0

FS
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SIO_000300: 2.597e0

QD
type: SiteQuality
SIO_000300: 1.812e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 4.259e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

DP
type: SiteQuality
SIO_000300: 1.409796e6

GenotypeDepth
all individuals: 18889
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 847
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variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6751
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
all individuals: 6420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 876
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variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32327
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56556
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.224289911851126e-4
allele num: 8168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.384789e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.424e0

FS
type: SiteQuality
SIO_000300: 3.567e0

QD
type: SiteQuality
SIO_000300: 1.22e1

MQ
type: SiteQuality
SIO_000300: 4.022e1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 143
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variant carriers: 0

GenotypeDepth
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 6420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
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variant carriers: 0

GenotypeQuality
all individuals: 876
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variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 7337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 6751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 4.005340453938585e-4
allele num: 7490
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56556
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 1.384789e6

FS
type: SiteQuality
SIO_000300: 3.567e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

MQ
type: SiteQuality
SIO_000300: 4.022e1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 922
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variant carriers: 30

GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 547
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 7.105835144624645e-4
allele num: 47848
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.677852348993289e-3
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -8.699999999999999e-3

ClippingRankSum
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QD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.909e1

ReadPosRankSum
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SIO_000300: 3.17e-1

VQSLOD
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SIO_000300: -2.62e0

BaseQRankSum
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SIO_000300: -3.038e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

DP
type: SiteQuality
SIO_000300: 1.06849e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 194
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.541425231269696e-5
allele num: 39348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3204
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.98e-2

FS
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VQSLOD
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SIO_000300: -3.434e0

MQRankSum
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DP
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SIO_000300: 7.80547e5

MQ
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SIO_000300: 3.4e1

ClippingRankSum
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SIO_000300: -7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

BaseQRankSum
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SIO_000300: 5.43e0

QD
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SIO_000300: 1.382e1

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
all individuals: 191
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GenotypeQuality
all individuals: 20174
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 3731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.367398917542184e-5
allele num: 31410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2524
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 6.29794e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.65e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

MQ
type: SiteQuality
SIO_000300: 3.2e1

VQSLOD
type: SiteQuality
SIO_000300: -4.566e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13215
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4703
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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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: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.217358865953743e-4
allele num: 8042
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.95159386068477e-4
allele num: 3388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28470
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

FS
type: SiteQuality
SIO_000300: 2.881e0

QD
type: SiteQuality
SIO_000300: 8.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.97e-2

DP
type: SiteQuality
SIO_000300: 5.96363e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

MQ
type: SiteQuality
SIO_000300: 3.14e1

VQSLOD
type: SiteQuality
SIO_000300: -4.349e0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4477
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GenotypeQuality
all individuals: 888
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.671880737313652e-5
allele num: 27234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1992
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.90894e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -5.006e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 6.44e0

MQ
type: SiteQuality
SIO_000300: 2.809e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

GenotypeQuality
all individuals: 1190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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
all individuals: 20022
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GenotypeQuality
all individuals: 1733
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.154375118289067e-5
allele num: 63404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15302
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.593e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.568e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

DP
type: SiteQuality
SIO_000300: 2.278366e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.314e0

GenotypeQuality
all individuals: 18007
bin: 9.75e1
variant carriers: 10920

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 97

GenotypeQuality
all individuals: 315
bin: 7.5e0
variant carriers: 34

GenotypeQuality
all individuals: 3592
bin: 2.25e1
variant carriers: 54

GenotypeQuality
all individuals: 20022
bin: 6.25e1
variant carriers: 92

GenotypeQuality
all individuals: 1568
bin: 5.25e1
variant carriers: 94

GenotypeQuality
all individuals: 1447
bin: 7.25e1
variant carriers: 59

GenotypeQuality
all individuals: 511
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variant carriers: 66

GenotypeQuality
all individuals: 1190
bin: 3.25e1
variant carriers: 71

GenotypeQuality
all individuals: 229
bin: 2.5e0
variant carriers: 22

GenotypeQuality
all individuals: 872
bin: 4.25e1
variant carriers: 64

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 55

GenotypeQuality
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variant carriers: 31

GenotypeQuality
all individuals: 1283
bin: 3.75e1
variant carriers: 76

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 82

GenotypeQuality
all individuals: 1130
bin: 8.25e1
variant carriers: 107

GenotypeQuality
all individuals: 4423
bin: 6.75e1
variant carriers: 92

GenotypeQuality
all individuals: 1733
bin: 4.75e1
variant carriers: 73

European (Non-Finnish)
type: Population
allele count: 8435
allele frequency: 1.330357706138414e-1
allele num: 63404
num of homozygotes: 496

South Asian
type: Population
allele count: 2362
allele frequency: 1.543589073323748e-1
allele num: 15302
num of homozygotes: 170

Latino
type: Population
allele count: 705
allele frequency: 6.476207973544001e-2
allele num: 10886
num of homozygotes: 35

Other
type: Population
allele count: 115
allele frequency: 1.359338061465721e-1
allele num: 846
num of homozygotes: 9

African
type: Population
allele count: 347
allele frequency: 3.876228775692583e-2
allele num: 8952
num of homozygotes: 25

East Asian
type: Population
allele count: 75
allele frequency: 8.913715236510578e-3
allele num: 8414
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 629
allele frequency: 1.007689842999039e-1
allele num: 6242
num of homozygotes: 30

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.568e-1

DP
type: SiteQuality
SIO_000300: 2.278366e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 4.593e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574753551069258e-5
allele num: 63502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.083e1

VQSLOD
type: SiteQuality
SIO_000300: -2.168e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

ReadPosRankSum
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SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 2.138636e6

QD
type: SiteQuality
SIO_000300: 1.047e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4443
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GenotypeQuality
all individuals: 1950
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575100806451613e-5
allele num: 63488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.317349492820445e-4
allele num: 15182
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.11681929863748e-4
allele num: 8954
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.85e0

MQ
type: SiteQuality
SIO_000300: 4.347e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 1.5826e1

DP
type: SiteQuality
SIO_000300: 2.138297e6

QD
type: SiteQuality
SIO_000300: 7.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5449
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GenotypeQuality
all individuals: 9135
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variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10904
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: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575001575001575e-5
allele num: 63492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8946
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.59e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.098e0

FS
type: SiteQuality
SIO_000300: 1.075e0

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.431e0

DP
type: SiteQuality
SIO_000300: 2.138007e6

GenotypeQuality
all individuals: 1420
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 25521
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1277
bin: 3.25e1
variant carriers: 8

GenotypeQuality
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bin: 5.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4441
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 313
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 9414
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variant carriers: 513

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 1901
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variant carriers: 5

GenotypeQuality
all individuals: 935
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 910
bin: 4.25e1
variant carriers: 6

GenotypeQuality
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bin: 1.25e1
variant carriers: 3

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 7

GenotypeQuality
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bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1163
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 2.202238942925307e-3
allele num: 10898
num of homozygotes: 0

African
type: Population
allele count: 586
allele frequency: 6.568034073077786e-2
allele num: 8922
num of homozygotes: 53

Other
type: Population
allele count: 2
allele frequency: 2.403846153846154e-3
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.205627501024041e-4
allele num: 63474
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.493e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

DP
type: SiteQuality
SIO_000300: 2.137841e6

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.446e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 1898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.125619090499775e-4
allele num: 8884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63450
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.435e0

DP
type: SiteQuality
SIO_000300: 2.130365e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

FS
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.352e0

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.783e0

MQ
type: SiteQuality
SIO_000300: 4.615e1

GenotypeQuality
all individuals: 5270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4784
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8949
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29089
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1580
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variant carriers: 0

GenotypeQuality
all individuals: 1293
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variant carriers: 0

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.19047619047619e-4
allele num: 8400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63352
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 2.136212e6

MQ
type: SiteQuality
SIO_000300: 4.392e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.472e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.032e0

VQSLOD
type: SiteQuality
SIO_000300: -2.778e0

QD
type: SiteQuality
SIO_000300: 1.255e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.59e-1

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5078
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variant carriers: 0

GenotypeQuality
all individuals: 8942
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variant carriers: 0

GenotypeQuality
all individuals: 1037
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variant carriers: 0

GenotypeQuality
all individuals: 489
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GenotypeQuality
all individuals: 1683
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variant carriers: 0

GenotypeQuality
all individuals: 393
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GenotypeQuality
all individuals: 1098
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variant carriers: 0

GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 643
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 829
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variant carriers: 0

GenotypeQuality
all individuals: 5167
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 576
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30451
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GenotypeQuality
all individuals: 1535
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15114
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63256
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.159e0

FS
type: SiteQuality
SIO_000300: 3.256e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

DP
type: SiteQuality
SIO_000300: 2.141684e6

QD
type: SiteQuality
SIO_000300: 1.482e1

MQ
type: SiteQuality
SIO_000300: 4.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1447
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GenotypeQuality
all individuals: 637
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.591596371160274e-5
allele num: 62830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15030
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.446691176470588e-4
allele num: 8704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.137071e6

MQ
type: SiteQuality
SIO_000300: 4.676e1

VQSLOD
type: SiteQuality
SIO_000300: -5.465e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 1.149e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62726
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.301495972382048e-4
allele num: 8690
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15008
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 4.392e1

QD
type: SiteQuality
SIO_000300: 2.349e1

VQSLOD
type: SiteQuality
SIO_000300: -1.268e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.135033e6

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: 560
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.633453119895459e-4
allele num: 6122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

DP
type: SiteQuality
SIO_000300: 2.123763e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 4.924e1

QD
type: SiteQuality
SIO_000300: 3.81e0