6-170176046-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176046
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176046
    reference: chr 6
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1027A>G
  hgvsp: ENSP00000375945.4:p.Asn343Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1405A>G
  hgvsp: ENSP00000397661.2:p.Asn469Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1405A>G
  hgvsp: ENSP00000355735.3:p.Asn469Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1503A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1405A>G
  hgvsp: ENSP00000355734.1:p.Asn469Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.997A>G
  hgvsp: ENSP00000468240.1:p.Asn333Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.447A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.73A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn469Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-170176050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176050
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176050
    reference: chr 6
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1409C>T
  hgvsp: ENSP00000355735.3:p.Ser470Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1409C>T
  hgvsp: ENSP00000355734.1:p.Ser470Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1001C>T
  hgvsp: ENSP00000468240.1:p.Ser334Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1409C>T
  hgvsp: ENSP00000397661.2:p.Ser470Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.77C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1031C>T
  hgvsp: ENSP00000375945.4:p.Ser344Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.451C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1507C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6075
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser470Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

6-170176060-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176060
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176060
    reference: chr 6
allele count: 25
allele frequency: 2.063966448161419e-4
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.461T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1419T>C
  hgvsp: ENST00000366772.2:c.1419T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1419T>C
  hgvsp: ENST00000418781.3:c.1419T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.87T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1041T>C
  hgvsp: ENST00000392095.4:c.1041T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1419T>C
  hgvsp: ENST00000366773.3:c.1419T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1517T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1011T>C
  hgvsp: ENST00000588451.1:c.1011T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34784
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn473Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

6-170176062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176062
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176062
    reference: chr 6
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1421C>T
  hgvsp: ENSP00000397661.2:p.Ala474Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1421C>T
  hgvsp: ENSP00000355735.3:p.Ala474Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1013C>T
  hgvsp: ENSP00000468240.1:p.Ala338Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1043C>T
  hgvsp: ENSP00000375945.4:p.Ala348Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1421C>T
  hgvsp: ENSP00000355734.1:p.Ala474Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.89C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1519C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.463C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala474Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

6-170176067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176067
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176067
    reference: chr 6
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1524C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1426C>T
  hgvsp: ENSP00000355734.1:p.His476Tyr
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1018C>T
  hgvsp: ENSP00000468240.1:p.His340Tyr
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1426C>T
  hgvsp: ENSP00000397661.2:p.His476Tyr
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1048C>T
  hgvsp: ENSP00000375945.4:p.His350Tyr
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.468C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.94C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1426C>T
  hgvsp: ENSP00000355735.3:p.His476Tyr
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His476Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS

6-170176071-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176071
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176069
    reference: chr 6
allele count: 2
allele frequency: 1.648940555692967e-5
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1432_1433delTT
  hgvsp: ENSP00000355735.3:p.Leu478AspfsTer7
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.100_101delTT
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1530_1531delTT
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1024_1025delTT
  hgvsp: ENSP00000468240.1:p.Leu342AspfsTer7
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1054_1055delTT
  hgvsp: ENSP00000375945.4:p.Leu352AspfsTer7
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1432_1433delTT
  hgvsp: ENSP00000355734.1:p.Leu478AspfsTer7
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1432_1433delTT
  hgvsp: ENSP00000397661.2:p.Leu478AspfsTer7
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.474_475delTT
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2991
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6211
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu478AspfsTer7
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: CTT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

6-170176072-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176072
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176072
    reference: chr 6
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.99T>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1023T>G
  hgvsp: ENST00000588451.1:c.1023T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1053T>G
  hgvsp: ENST00000392095.4:c.1053T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.473T>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1431T>G
  hgvsp: ENST00000366772.2:c.1431T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1431T>G
  hgvsp: ENST00000418781.3:c.1431T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1431T>G
  hgvsp: ENST00000366773.3:c.1431T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1529T>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser477Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-170176087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176087
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176087
    reference: chr 6
allele count: 57
allele frequency: 4.697931261847853e-4
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1446G>A
  hgvsp: ENSP00000397661.2:p.Met482Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1068G>A
  hgvsp: ENSP00000375945.4:p.Met356Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1446G>A
  hgvsp: ENSP00000355735.3:p.Met482Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1446G>A
  hgvsp: ENSP00000355734.1:p.Met482Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.488G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1038G>A
  hgvsp: ENSP00000468240.1:p.Met346Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.114G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1544G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33884
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34736
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met482Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

6-170176089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176089
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176089
    reference: chr 6
allele count: 5
allele frequency: 4.120788554097712e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1448C>T
  hgvsp: ENSP00000355735.3:p.Thr483Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1448C>T
  hgvsp: ENSP00000355734.1:p.Thr483Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.116C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1448C>T
  hgvsp: ENSP00000397661.2:p.Thr483Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1546C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1040C>T
  hgvsp: ENSP00000468240.1:p.Thr347Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1070C>T
  hgvsp: ENSP00000375945.4:p.Thr357Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.490C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7485
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34719
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr483Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

6-170176090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176090
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176090
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1071G>A
  hgvsp: ENST00000392095.4:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1449G>A
  hgvsp: ENST00000366772.2:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.117G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1449G>A
  hgvsp: ENST00000366773.3:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1041G>A
  hgvsp: ENST00000588451.1:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1547G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1449G>A
  hgvsp: ENST00000418781.3:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.491G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7490
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr483Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-170176094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176094
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176094
    reference: chr 6
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1075G>A
  hgvsp: ENSP00000375945.4:p.Glu359Lys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1453G>A
  hgvsp: ENSP00000355734.1:p.Glu485Lys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.121G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1551G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.495G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1045G>A
  hgvsp: ENSP00000468240.1:p.Glu349Lys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1453G>A
  hgvsp: ENSP00000355735.3:p.Glu485Lys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1453G>A
  hgvsp: ENSP00000397661.2:p.Glu485Lys
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34736
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3662
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6257
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu485Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

6-170176096-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176096
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176096
    reference: chr 6
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.123G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1047G>A
  hgvsp: ENST00000588451.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1455G>A
  hgvsp: ENST00000366773.3:c.1455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1455G>A
  hgvsp: ENST00000418781.3:c.1455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1077G>A
  hgvsp: ENST00000392095.4:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1455G>A
  hgvsp: ENST00000366772.2:c.1455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.497G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1553G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu485Glu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-170176096-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176096
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176096
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1553G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.123G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1047G>T
  hgvsp: ENSP00000468240.1:p.Glu349Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1455G>T
  hgvsp: ENSP00000355734.1:p.Glu485Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1455G>T
  hgvsp: ENSP00000397661.2:p.Glu485Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1455G>T
  hgvsp: ENSP00000355735.3:p.Glu485Asp
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.497G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1077G>T
  hgvsp: ENSP00000375945.4:p.Glu359Asp
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu485Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

6-170176099-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176099
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176099
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1080G>T
  hgvsp: ENST00000392095.4:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1458G>T
  hgvsp: ENST00000366772.2:c.1458G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1458G>T
  hgvsp: ENST00000418781.3:c.1458G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.500G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1458G>T
  hgvsp: ENST00000366773.3:c.1458G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1050G>T
  hgvsp: ENST00000588451.1:c.1050G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.126G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1556G>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu486Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

6-170176101-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176101
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176101
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1558A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.128A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1460A>T
  hgvsp: ENSP00000355734.1:p.Tyr487Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1052A>T
  hgvsp: ENSP00000468240.1:p.Tyr351Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.502A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1082A>T
  hgvsp: ENSP00000375945.4:p.Tyr361Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1460A>T
  hgvsp: ENSP00000397661.2:p.Tyr487Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1460A>T
  hgvsp: ENSP00000355735.3:p.Tyr487Phe
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34716
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3002
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr487Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

6-170176104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176104
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176104
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1463A>G
  hgvsp: ENSP00000355734.1:p.His488Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.131A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.505A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1561A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1055A>G
  hgvsp: ENSP00000468240.1:p.His352Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1463A>G
  hgvsp: ENSP00000355735.3:p.His488Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1085A>G
  hgvsp: ENSP00000375945.4:p.His362Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1463A>G
  hgvsp: ENSP00000397661.2:p.His488Arg
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His488Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

6-170176108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176108
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176108
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.135T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1059T>C
  hgvsp: ENST00000588451.1:c.1059T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1565T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1467T>C
  hgvsp: ENST00000366773.3:c.1467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.509T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1467T>C
  hgvsp: ENST00000418781.3:c.1467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1089T>C
  hgvsp: ENST00000392095.4:c.1089T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1467T>C
  hgvsp: ENST00000366772.2:c.1467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6262
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His489His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-170176109-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176109
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176109
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1468A>G
  hgvsp: ENSP00000355735.3:p.Met490Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1090A>G
  hgvsp: ENSP00000375945.4:p.Met364Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1468A>G
  hgvsp: ENSP00000397661.2:p.Met490Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1468A>G
  hgvsp: ENSP00000355734.1:p.Met490Val
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.136A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1566A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.510A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1060A>G
  hgvsp: ENSP00000468240.1:p.Met354Val
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met490Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-170176113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176113
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176113
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.514C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1472C>T
  hgvsp: ENSP00000355734.1:p.Pro491Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.140C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1094C>T
  hgvsp: ENSP00000375945.4:p.Pro365Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1472C>T
  hgvsp: ENSP00000397661.2:p.Pro491Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1064C>T
  hgvsp: ENSP00000468240.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1472C>T
  hgvsp: ENSP00000355735.3:p.Pro491Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1570C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6265
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro491Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-170176121-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176121
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176121
    reference: chr 6
allele count: 90
allele frequency: 7.417052628108981e-4
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1102C>G
  hgvsp: ENSP00000375945.4:p.Arg368Gly
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.522C>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1480C>G
  hgvsp: ENSP00000355734.1:p.Arg494Gly
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.148C>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1072C>G
  hgvsp: ENSP00000468240.1:p.Arg358Gly
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1480C>G
  hgvsp: ENSP00000397661.2:p.Arg494Gly
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1578C>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1480C>G
  hgvsp: ENSP00000355735.3:p.Arg494Gly
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7477
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg494Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

6-170176121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176121
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176121
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1072C>T
  hgvsp: ENSP00000468240.1:p.Arg358Cys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1480C>T
  hgvsp: ENSP00000397661.2:p.Arg494Cys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1480C>T
  hgvsp: ENSP00000355734.1:p.Arg494Cys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1578C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1480C>T
  hgvsp: ENSP00000355735.3:p.Arg494Cys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1102C>T
  hgvsp: ENSP00000375945.4:p.Arg368Cys
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.148C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.522C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3662
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg494Cys
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS

6-170176122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176122
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176122
    reference: chr 6
allele count: 3
allele frequency: 2.472432378974435e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1481G>A
  hgvsp: ENSP00000397661.2:p.Arg494His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1579G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1073G>A
  hgvsp: ENSP00000468240.1:p.Arg358His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1103G>A
  hgvsp: ENSP00000375945.4:p.Arg368His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.149G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.523G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1481G>A
  hgvsp: ENSP00000355734.1:p.Arg494His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1481G>A
  hgvsp: ENSP00000355735.3:p.Arg494His
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg494His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-170176122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176122
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176122
    reference: chr 6
allele count: 3
allele frequency: 2.472432378974435e-5
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1103G>C
  hgvsp: ENSP00000375945.4:p.Arg368Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1481G>C
  hgvsp: ENSP00000355734.1:p.Arg494Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1481G>C
  hgvsp: ENSP00000397661.2:p.Arg494Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1073G>C
  hgvsp: ENSP00000468240.1:p.Arg358Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1481G>C
  hgvsp: ENSP00000355735.3:p.Arg494Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1579G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.149G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.523G>C
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33640
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34615
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg494Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

6-170176135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176135
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176135
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1592G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.162G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1494G>A
  hgvsp: ENST00000418781.3:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1116G>A
  hgvsp: ENST00000392095.4:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1494G>A
  hgvsp: ENST00000366772.2:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1086G>A
  hgvsp: ENST00000588451.1:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1494G>A
  hgvsp: ENST00000366773.3:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.536G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys498Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

6-170176144-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176144
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176143
    reference: chr 6
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1504delC
  hgvsp: ENSP00000355734.1:p.Arg502ValfsTer13
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1602delC
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1096delC
  hgvsp: ENSP00000468240.1:p.Arg366ValfsTer55
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.172delC
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.546delC
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1126delC
  hgvsp: ENSP00000375945.4:p.Arg376ValfsTer55
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1504delC
  hgvsp: ENSP00000355735.3:p.Arg502ValfsTer55
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1504delC
  hgvsp: ENSP00000397661.2:p.Arg502ValfsTer16
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg502ValfsTer55
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TC
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-170176146-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176146
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176146
    reference: chr 6
allele count: 9519
allele frequency: 7.848003165913663e-2
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1127G>A
  hgvsp: ENSP00000375945.4:p.Arg376His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1505G>A
  hgvsp: ENSP00000355735.3:p.Arg502His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1505G>A
  hgvsp: ENSP00000397661.2:p.Arg502His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1505G>A
  hgvsp: ENSP00000355734.1:p.Arg502His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1097G>A
  hgvsp: ENSP00000468240.1:p.Arg366His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.173G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.547G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1603G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 611
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 2271
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 2.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 728
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 28509
  bin: 2.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 3.25e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 645
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 705
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 711
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 420
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 356
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 538
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.75e1
  variant carriers: 498
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 610
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14387
  bin: 9.75e1
  variant carriers: 9051
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg502His
num of homozygotes: 445
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-170176146-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176146
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176146
    reference: chr 6
allele count: 2
allele frequency: 1.648913366091746e-5
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1505G>C
  hgvsp: ENSP00000355734.1:p.Arg502Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.173G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1505G>C
  hgvsp: ENSP00000355735.3:p.Arg502Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1097G>C
  hgvsp: ENSP00000468240.1:p.Arg366Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1127G>C
  hgvsp: ENSP00000375945.4:p.Arg376Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1505G>C
  hgvsp: ENSP00000397661.2:p.Arg502Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.547G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1603G>C
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg502Pro
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

6-170176148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176148
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176148
    reference: chr 6
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.175C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1605C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1507C>T
  hgvsp: ENSP00000355734.1:p.Leu503Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1099C>T
  hgvsp: ENSP00000468240.1:p.Leu367Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1129C>T
  hgvsp: ENSP00000375945.4:p.Leu377Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1507C>T
  hgvsp: ENSP00000355735.3:p.Leu503Phe
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.549C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1507C>T
  hgvsp: ENSP00000397661.2:p.Leu503Phe
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu503Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-170176154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176154
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176154
    reference: chr 6
allele count: 52
allele frequency: 4.288589054201168e-4
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1135A>G
  hgvsp: ENSP00000375945.4:p.Thr379Ala
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1513A>G
  hgvsp: ENSP00000355734.1:p.Thr505Ala
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1105A>G
  hgvsp: ENSP00000468240.1:p.Thr369Ala
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.555A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1513A>G
  hgvsp: ENSP00000397661.2:p.Thr505Ala
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1611A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1513A>G
  hgvsp: ENSP00000355735.3:p.Thr505Ala
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.181A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12531
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3522
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr505Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-170176160-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176160
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176160
    reference: chr 6
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1617A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1111A>C
  hgvsp: ENSP00000468240.1:p.Thr371Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1519A>C
  hgvsp: ENSP00000397661.2:p.Thr507Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.187A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1141A>C
  hgvsp: ENSP00000375945.4:p.Thr381Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1519A>C
  hgvsp: ENSP00000355734.1:p.Thr507Pro
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.561A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1519A>C
  hgvsp: ENSP00000355735.3:p.Thr507Pro
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30204
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr507Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

6-170176161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176161
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176161
    reference: chr 6
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520C>T
  hgvsp: ENSP00000355735.3:p.Thr507Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520C>T
  hgvsp: ENSP00000355734.1:p.Thr507Ile
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142C>T
  hgvsp: ENSP00000375945.4:p.Thr381Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112C>T
  hgvsp: ENSP00000468240.1:p.Thr371Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520C>T
  hgvsp: ENSP00000397661.2:p.Thr507Ile
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr507Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

6-170176161-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176161
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176161
    reference: chr 6
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520C>G
  hgvsp: ENSP00000355734.1:p.Thr507Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520C>G
  hgvsp: ENSP00000397661.2:p.Thr507Ser
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188C>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112C>G
  hgvsp: ENSP00000468240.1:p.Thr371Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562C>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142C>G
  hgvsp: ENSP00000375945.4:p.Thr381Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520C>G
  hgvsp: ENSP00000355735.3:p.Thr507Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618C>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr507Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

6-170176162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176162
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176162
    reference: chr 6
allele count: 5
allele frequency: 4.12657015994586e-5
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+1G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+1G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10766
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1520+1G>A
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

6-170176175-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176175
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176175
    reference: chr 6
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+14C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+14C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10758
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-170176177-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176177
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176177
    reference: chr 6
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+16T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+16T>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10759
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
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: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-170176178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176178
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176178
    reference: chr 6
allele count: 2
allele frequency: 1.651773178507128e-5
allele num: 121082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+17C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+17C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-170176192-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176192
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176192
    reference: chr 6
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+31A>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+31A>C
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3487
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10762
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-170176196-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176196
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176196
    reference: chr 6
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+35A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+35A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26899
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3477
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10764
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-170176197-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176197
    reference: chr 6
allele count: 6
allele frequency: 4.959169504413661e-5
allele num: 120988
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+36T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+36T>C
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11955
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10770
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 27974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-170176200-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176200
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176200
    reference: chr 6
allele count: 17
allele frequency: 1.405400042988707e-4
allele num: 120962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+39A>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+39A>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6575
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

6-170176210-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176210
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176210
    reference: chr 6
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1520+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.188+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1520+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1142+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.562+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1618+49T>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1112+49T>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26559
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10775
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

6-170176380-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176380
    reference: chr 6
allele count: 1
allele frequency: 5.137162231583274e-5
allele num: 19466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-171A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+219A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-171A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-171A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-50A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-171A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-171A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-171A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25309
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

6-170176387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176387
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176387
    reference: chr 6
allele count: 1
allele frequency: 5.178127589063794e-5
allele num: 19312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-43G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-164G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-164G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-164G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+226G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-164G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-164G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-164G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

6-170176392-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176392
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 19250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+231T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-159T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-38T>C
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-170176399-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176399
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176399
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 19222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+238C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-152C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-31C>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30466
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

6-170176406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176406
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176406
    reference: chr 6
allele count: 10
allele frequency: 5.188875051888751e-4
allele num: 19272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-145C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-24C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-145C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-145C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-145C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-145C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+245C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-145C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

6-170176407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176407
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176407
    reference: chr 6
allele count: 6095
allele frequency: 3.023613453715646e-1
allele num: 20158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+246G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-144G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-144G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-144G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-144G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-23G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-144G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-144G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 7.5e0
  variant carriers: 2716
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 380
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 392
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 452
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 706
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 512
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.75e1
  variant carriers: 398
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 25104
  bin: 2.5e0
  variant carriers: 2078
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 316
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.75e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 6.75e1
  variant carriers: 99
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 616
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 2.25e1
  variant carriers: 513
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 285
num of homozygotes: 966
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

6-170176415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176415
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176415
    reference: chr 6
allele count: 1
allele frequency: 4.99001996007984e-5
allele num: 20040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-136C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-15C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+254C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-136C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-136C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-136C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-136C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-136C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-170176416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176416
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176416
    reference: chr 6
allele count: 1
allele frequency: 4.970178926441352e-5
allele num: 20120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+255G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-135G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1521-14G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-135G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-135G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-135G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-135G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-135G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-170176439-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176439
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176439
    reference: chr 6
allele count: 1
allele frequency: 4.841677156967173e-5
allele num: 20654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1530C>A
  hgvsp: ENSP00000355734.1:p.Ser510Arg
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-112C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-112C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-112C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-112C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-112C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+278C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-112C>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser510Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

6-170176439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176439
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176439
    reference: chr 6
allele count: 8
allele frequency: 3.873341725573739e-4
allele num: 20654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+278C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-112C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1530C>T
  hgvsp: ENST00000366772.2:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9181
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33912
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6259
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30864
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 6.75e1
  variant carriers: 5
hgvs: p.Ser510Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

6-170176442-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176442
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176442
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 20988
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1533T>C
  hgvsp: ENST00000366772.2:c.1533T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-109T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+281T>C
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33786
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp511Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

6-170176444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176444
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176444
    reference: chr 6
allele count: 9
allele frequency: 4.276753468922258e-4
allele num: 21044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+283C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-107C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1535C>T
  hgvsp: ENSP00000355734.1:p.Thr512Met
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10620
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33573
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr512Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

6-170176445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176445
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176445
    reference: chr 6
allele count: 181
allele frequency: 8.526474467684191e-3
allele num: 21228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-106G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1536G>A
  hgvsp: ENST00000366772.2:c.1536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-106G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-106G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+284G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-106G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-106G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-106G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 7.5e0
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 33207
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 9.75e1
  variant carriers: 181
hgvs: p.Thr512Thr
num of homozygotes: 2
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

6-170176447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176447
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176447
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 21312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-104C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+286C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-104C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1538C>T
  hgvsp: ENSP00000355734.1:p.Pro513Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-104C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-104C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-104C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-104C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33023
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11890
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9011
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro513Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-170176448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176448
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176448
    reference: chr 6
allele count: 7
allele frequency: 3.276846737196892e-4
allele num: 21362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-103G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-103G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-103G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+287G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-103G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-103G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1539G>A
  hgvsp: ENST00000366772.2:c.1539G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-103G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12469
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32699
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro513Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-170176452-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176452
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176452
    reference: chr 6
allele count: 1
allele frequency: 4.609569466211856e-5
allele num: 21694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-99G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1543G>T
  hgvsp: ENSP00000355734.1:p.Ala515Ser
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-99G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-99G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-99G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+291G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-99G>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-99G>T
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30025
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11799
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3839
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala515Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

6-170176460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176460
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176460
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 22378
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-91T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-91T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1551T>C
  hgvsp: ENST00000366772.2:c.1551T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-91T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+299T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-91T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-91T>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-91T>C
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28930
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27782
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Ala517Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-170176462-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176462
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176462
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 22514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1553C>A
  hgvsp: ENSP00000355734.1:p.Pro518His
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-89C>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+301C>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28219
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14588
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro518His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-170176467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176467
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176467
    reference: chr 6
allele count: 8976
allele frequency: 3.248877949905893e-1
allele num: 27628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1558A>G
  hgvsp: ENSP00000355734.1:p.Lys520Glu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-84A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+306A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.25e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 1.25e1
  variant carriers: 2452
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 18520
  bin: 2.5e0
  variant carriers: 1870
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 2.75e1
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 9.75e1
  variant carriers: 2274
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 7.5e0
  variant carriers: 7853
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 131
genotype quality: GenotypeQuality
  all individuals: 10908
  bin: 2.25e1
  variant carriers: 1048
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 3.25e1
  variant carriers: 282
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 9.25e1
  variant carriers: 783
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 6.25e1
  variant carriers: 521
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 1.25e1
  variant carriers: 686
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 1.75e1
  variant carriers: 1099
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 128
hgvs: p.Lys520Glu
num of homozygotes: 1271
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

6-170176470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176470
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176470
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 27458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-81C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1561C>T
  hgvsp: ENSP00000355734.1:p.Pro521Ser
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+309C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21326
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro521Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

6-170176471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176471
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176471
    reference: chr 6
allele count: 1
allele frequency: 3.636628118408612e-5
allele num: 27498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1562C>T
  hgvsp: ENSP00000355734.1:p.Pro521Leu
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-80C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+310C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23914
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21056
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5640
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19023
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro521Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

6-170176472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176472
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176472
    reference: chr 6
allele count: 2
allele frequency: 7.248477819657872e-5
allele num: 27592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-79G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-79G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-79G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+311G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-79G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1563G>A
  hgvsp: ENST00000366772.2:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-79G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-79G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24334
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18693
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro521Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

6-170176487-CAGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176484
    reference: chr 6
allele count: 1
allele frequency: 3.232270993600103e-5
allele num: 30938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1581_1583delAAG
  hgvsp: ENSP00000355734.1:p.Arg529del
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-61_563-59delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+329_1520+331delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-61_1619-59delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-61_1521-59delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-61_189-59delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-61_1143-59delAAG
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-61_1113-59delAAG
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29551
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24926
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg529del
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: CAGA
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

6-170176488-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176488
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176488
    reference: chr 6
allele count: 9
allele frequency: 2.881106344836417e-4
allele num: 31238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1579A>G
  hgvsp: ENSP00000355734.1:p.Arg527Gly
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-63A>G
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+327A>G
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30075
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg527Gly
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: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-170176493-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176493
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176493
    reference: chr 6
allele count: 1
allele frequency: 3.063913229977327e-5
allele num: 32638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1584G>A
  hgvsp: ENST00000366772.2:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-58G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+332G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11431
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg528Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

6-170176495-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176495
    reference: chr 6
allele count: 1
allele frequency: 3.009691205682297e-5
allele num: 33226
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-56G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-56G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1586G>C
  hgvsp: ENSP00000355734.1:p.Arg529Thr
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+334G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-56G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-56G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-56G>C
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-56G>C
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32339
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10621
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg529Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

6-170176495-GAGTGAGGCCCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176484
    reference: chr 6
allele count: 2
allele frequency: 6.019382411364594e-5
allele num: 33226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsp: ENSP00000355734.1:p.Val530TyrfsTer32
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val530TyrfsTer32
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: GAGTGAGGCCCA
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

6-170176497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176497
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176497
    reference: chr 6
allele count: 1
allele frequency: 2.95124542556959e-5
allele num: 33884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+336G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-54G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-54G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-54G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-54G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-54G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1588G>A
  hgvsp: ENSP00000355734.1:p.Val530Met
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-54G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3817
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9908
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val530Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

6-170176502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176502
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176502
    reference: chr 6
allele count: 1
allele frequency: 2.725686873092019e-5
allele num: 36688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-49G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-49G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1593G>A
  hgvsp: ENST00000366772.2:c.1593G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-49G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-49G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-49G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+341G>A
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-49G>A
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31428
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3821
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg531Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

6-170176505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 170176505
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 170176505
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 38792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000468240
  ensembl transcript: ENST00000588451
  gene symbol: ERMARD
  hgvsc: ENST00000588451.1:c.1113-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000366771
  gene symbol: ERMARD
  hgvsc: ENST00000366771.1:n.1619-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000477995
  gene symbol: ERMARD
  hgvsc: ENST00000477995.1:n.189-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000375945
  ensembl transcript: ENST00000392095
  gene symbol: ERMARD
  hgvsc: ENST00000392095.4:c.1143-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl transcript: ENST00000492738
  gene symbol: ERMARD
  hgvsc: ENST00000492738.1:n.563-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355734
  ensembl transcript: ENST00000366772
  gene symbol: ERMARD
  hgvsc: ENST00000366772.2:c.1596C>T
  hgvsp: ENST00000366772.2:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000355735
  ensembl transcript: ENST00000366773
  gene symbol: ERMARD
  hgvsc: ENST00000366773.3:c.1521-46C>T
  variant of: http://identifiers.org/hgnc/21056
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130023
  ensembl protein: ENSP00000397661
  ensembl transcript: ENST00000418781
  gene symbol: ERMARD
  hgvsc: ENST00000418781.3:c.1520+344C>T
  variant of: http://identifiers.org/hgnc/21056
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34411
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3825
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1596C>T
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7323
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6074
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 4.653e0

QD
type: SiteQuality
SIO_000300: 1.439e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.698355e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.19e-1

GenotypeQuality
all individuals: 2933
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 34785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.701185e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.87e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.56e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.21e-1

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

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

GenotypeQuality
all individuals: 1160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6121
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 7427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2974
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 12
allele frequency: 7.285089849441476e-4
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.652048540189835e-4
allele num: 66584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.343e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.69e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

DP
type: SiteQuality
SIO_000300: 1.707074e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

GenotypeQuality
all individuals: 6198
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7450
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34738
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3618
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.372e1

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

DP
type: SiteQuality
SIO_000300: 1.71213e6

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

GenotypeQuality
all individuals: 1421
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6207
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.97e0

QD
type: SiteQuality
SIO_000300: 1.189e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.625e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 1.713796e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34781
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 2.249e0

MQ
type: SiteQuality
SIO_000300: 6.067e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.714808e6

QD
type: SiteQuality
SIO_000300: 1.891e1

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7488
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34781
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6212
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2769
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.714764e6

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.035e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

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

GenotypeQuality
all individuals: 2780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7486
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6271
bin: 9.75e1
variant carriers: 57

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3651
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 55
allele frequency: 8.245877061469265e-4
allele num: 66700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

QD
type: SiteQuality
SIO_000300: 1.329e1

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.448e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.718364e6

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

GenotypeQuality
all individuals: 6251
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2781
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
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Other
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Latino
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South Asian
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African
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European (Non-Finnish)
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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East Asian
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African
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Other
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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DP
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BaseQRankSum
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QD
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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European (Non-Finnish)
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East Asian
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African
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QD
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DP
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FS
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.124e0

DP
type: SiteQuality
SIO_000300: 1.718828e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 1.528e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.339e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

FS
type: SiteQuality
SIO_000300: 1.0983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

DP
type: SiteQuality
SIO_000300: 1.718855e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 90

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 25
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GenotypeQuality
all individuals: 1177
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 31
allele frequency: 4.68702751738736e-3
allele num: 6614
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 8.694870026684257e-4
allele num: 66706
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.724118e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 6.62e0

QD
type: SiteQuality
SIO_000300: 1.394e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

VQSLOD
type: SiteQuality
SIO_000300: 6.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

DP
type: SiteQuality
SIO_000300: 1.724118e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.394e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

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
all individuals: 27
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GenotypeQuality
all individuals: 7482
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

DP
type: SiteQuality
SIO_000300: 1.722012e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.219e0

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49734656552634e-5
allele num: 66706
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.303e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

DP
type: SiteQuality
SIO_000300: 1.722012e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 3.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 20
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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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bin: 9.75e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.721577e6

FS
type: SiteQuality
SIO_000300: 1.764e0

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.094e0

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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bin: 8.25e1
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GenotypeQuality
all individuals: 3658
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.925298421255295e-4
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQ
type: SiteQuality
SIO_000300: 6.036e1

DP
type: SiteQuality
SIO_000300: 1.721263e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.391e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 2529
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 45
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variant carriers: 0

European (Finnish)
type: Population
allele count: 497
allele frequency: 7.516636418632788e-2
allele num: 6612
num of homozygotes: 20

Latino
type: Population
allele count: 371
allele frequency: 3.206568712186689e-2
allele num: 11570
num of homozygotes: 7

African
type: Population
allele count: 713
allele frequency: 6.863688871775125e-2
allele num: 10388
num of homozygotes: 35

Other
type: Population
allele count: 79
allele frequency: 8.738938053097345e-2
allele num: 904
num of homozygotes: 6

East Asian
type: Population
allele count: 1030
allele frequency: 1.191577973160574e-1
allele num: 8644
num of homozygotes: 83

European (Non-Finnish)
type: Population
allele count: 5521
allele frequency: 8.278602489128804e-2
allele num: 66690
num of homozygotes: 231

South Asian
type: Population
allele count: 1308
allele frequency: 7.934967240960931e-2
allele num: 16484
num of homozygotes: 63

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 6.49e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

DP
type: SiteQuality
SIO_000300: 2.209802e6

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14387
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GenotypeQuality
all individuals: 2529
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GenotypeQuality
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GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 38
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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: 4.75e1
variant carriers: 0

South Asian
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allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

QD
type: SiteQuality
SIO_000300: 1.419e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

DP
type: SiteQuality
SIO_000300: 2.209802e6

VQSLOD
type: SiteQuality
SIO_000300: 6.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.925415e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.954e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.441e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.722e0

MQRankSum
type: SiteQuality
SIO_000300: -2.52e0

FS
type: SiteQuality
SIO_000300: 6.652e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 52

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 51
allele frequency: 4.909510974201001e-3
allele num: 10388
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.927565e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

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
all individuals: 10766
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

DP
type: SiteQuality
SIO_000300: 1.923695e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

FS
type: SiteQuality
SIO_000300: 1.015e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2822
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GenotypeQuality
all individuals: 10765
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 1.923718e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-1

GenotypeQuality
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bin: 7.5e0
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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6847
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

DP
type: SiteQuality
SIO_000300: 1.923718e6

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.114e1

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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bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.046922608165753e-4
allele num: 16410
num of homozygotes: 1

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

VQSLOD
type: SiteQuality
SIO_000300: -7.22e-2

QD
type: SiteQuality
SIO_000300: 1.9e1

DP
type: SiteQuality
SIO_000300: 1.922701e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.290000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

FS
type: SiteQuality
SIO_000300: 3.86e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2815
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113964294448521e-5
allele num: 16356
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 8.912000000000001e0

DP
type: SiteQuality
SIO_000300: 1.916989e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.042e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.632e0

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
all individuals: 7
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GenotypeQuality
all individuals: 225
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.915055e6

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.976e0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 10761
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002101471029721e-5
allele num: 66620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

DP
type: SiteQuality
SIO_000300: 1.915446e6

MQ
type: SiteQuality
SIO_000300: 5.879e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 8.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.701e1

VQSLOD
type: SiteQuality
SIO_000300: -4.722e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.518e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.36e-1

DP
type: SiteQuality
SIO_000300: 1.906226e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.708e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
all individuals: 28124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.886e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.28e-2

DP
type: SiteQuality
SIO_000300: 1.903193e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.336e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.641e0

VQSLOD
type: SiteQuality
SIO_000300: -2.525e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 2.019e1

GenotypeQuality
all individuals: 2721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.011715229798738e-5
allele num: 66580
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

DP
type: SiteQuality
SIO_000300: 1.902506e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.342000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

GenotypeQuality
all individuals: 3475
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27184
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 385
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variant carriers: 0

GenotypeQuality
all individuals: 1693
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variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 10776
bin: 9.75e1
variant carriers: 17

East Asian
type: Population
allele count: 17
allele frequency: 1.96577243293247e-3
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.597e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

DP
type: SiteQuality
SIO_000300: 1.899494e6

QD
type: SiteQuality
SIO_000300: 1.315e1

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 578
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variant carriers: 0

GenotypeQuality
all individuals: 660
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 3489
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variant carriers: 0

GenotypeQuality
all individuals: 863
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variant carriers: 0

GenotypeQuality
all individuals: 2808
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variant carriers: 0

GenotypeQuality
all individuals: 1698
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variant carriers: 0

GenotypeQuality
all individuals: 2705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.182762458266353e-5
allele num: 16174
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.629e0

VQSLOD
type: SiteQuality
SIO_000300: -2.2e0

QD
type: SiteQuality
SIO_000300: 7.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.05e-1

DP
type: SiteQuality
SIO_000300: 1.897549e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeQuality
all individuals: 474
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6446
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2578
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GenotypeQuality
all individuals: 146
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variant carriers: 1

GenotypeQuality
all individuals: 308
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variant carriers: 2

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1864
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.243162605668821e-4
allele num: 8044
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 3.85711e5

VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1249
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 263
bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
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variant carriers: 0

GenotypeQuality
all individuals: 301
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variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.24750499001996e-4
allele num: 8016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1840
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.513e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.28e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.809e0

DP
type: SiteQuality
SIO_000300: 3.82713e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 560
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2280
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: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
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GenotypeQuality
all individuals: 402
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.95e0

DP
type: SiteQuality
SIO_000300: 3.81456e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeQuality
all individuals: 2625
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
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GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5083
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.909999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.83217e5

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2863
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1510
bin: 9.75e1
variant carriers: 11

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

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.258811681772407e-3
allele num: 7944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 5.325e0

VQSLOD
type: SiteQuality
SIO_000300: -1.392e0

DP
type: SiteQuality
SIO_000300: 3.89576e5

GenotypeQuality
all individuals: 7625
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 17735
bin: 7.5e0
variant carriers: 1002

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 264

GenotypeQuality
all individuals: 335
bin: 7.75e1
variant carriers: 113

GenotypeQuality
all individuals: 5111
bin: 9.75e1
variant carriers: 4777

GenotypeQuality
all individuals: 1547
bin: 1.25e1
variant carriers: 608

GenotypeQuality
all individuals: 272
bin: 5.25e1
variant carriers: 238

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 243

GenotypeQuality
all individuals: 511
bin: 2.75e1
variant carriers: 296

GenotypeQuality
all individuals: 314
bin: 3.25e1
variant carriers: 145

GenotypeQuality
all individuals: 2645
bin: 6.25e1
variant carriers: 199

GenotypeQuality
all individuals: 303
bin: 8.25e1
variant carriers: 189

African
type: Population
allele count: 1070
allele frequency: 5.032925682031985e-1
allele num: 2126
num of homozygotes: 249

European (Finnish)
type: Population
allele count: 35
allele frequency: 2.966101694915254e-1
allele num: 118
num of homozygotes: 1

Latino
type: Population
allele count: 172
allele frequency: 3.333333333333333e-1
allele num: 516
num of homozygotes: 24

European (Non-Finnish)
type: Population
allele count: 2180
allele frequency: 2.5841631104789e-1
allele num: 8436
num of homozygotes: 266

South Asian
type: Population
allele count: 2326
allele frequency: 2.896637608966376e-1
allele num: 8030
num of homozygotes: 371

East Asian
type: Population
allele count: 248
allele frequency: 3.406593406593407e-1
allele num: 728
num of homozygotes: 44

Other
type: Population
allele count: 64
allele frequency: 3.137254901960784e-1
allele num: 204
num of homozygotes: 11

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.696e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.208e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 4.63522e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28286
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.249063202598052e-4
allele num: 8006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.908e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.556e0

DP
type: SiteQuality
SIO_000300: 4.64984e5

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

VQSLOD
type: SiteQuality
SIO_000300: -1.589e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.34e-1

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.248751248751249e-4
allele num: 8008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 3.455e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.34e-2

DP
type: SiteQuality
SIO_000300: 4.67573e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.969e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.557885141294439e-4
allele num: 2194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.99541e5

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2731
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3234
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1701
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1917
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.740648379052369e-4
allele num: 8020
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 8.032128514056224e-3
allele num: 498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.124606387764283e-4
allele num: 8892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.99541e5

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2284
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9106
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.09316e5

QD
type: SiteQuality
SIO_000300: 2.582e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.29e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.125e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 31033
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3226
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1878
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7643
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.245019920318725e-4
allele num: 8032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 7.655293088363954e-4
allele num: 9144
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 4.359197907585005e-4
allele num: 2294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.516e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 5.13626e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 3.424e0

GenotypeQuality
all individuals: 8350
bin: 2.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1593
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 30909
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 19

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 13

GenotypeQuality
all individuals: 226
bin: 9.25e1
variant carriers: 14

GenotypeQuality
all individuals: 2007
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 387
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 356
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 407
bin: 7.75e1
variant carriers: 11

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 5.882352941176471e-3
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

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

African
type: Population
allele count: 174
allele frequency: 7.268170426065163e-2
allele num: 2394
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 3.256621797655232e-4
allele num: 9212
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.61e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.452e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

DP
type: SiteQuality
SIO_000300: 5.20993e5

GenotypeQuality
all individuals: 964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30935
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.25364e5

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 1.966e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 1916
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 30523
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 9255
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1784
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2073
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.458975634012929e-4
allele num: 8044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.073191672032625e-4
allele num: 9318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 5.30541e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.07e-2

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1564
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.048218029350105e-4
allele num: 9540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 3.274e0

QD
type: SiteQuality
SIO_000300: 1.099e1

MQ
type: SiteQuality
SIO_000300: 5.723e1

DP
type: SiteQuality
SIO_000300: 5.4475e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.86e-1

GenotypeQuality
all individuals: 14370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8106
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.67997e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.17e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.912e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.349e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3827
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27039
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 9.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.73635e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.11e-2

QD
type: SiteQuality
SIO_000300: 7.46e0

VQSLOD
type: SiteQuality
SIO_000300: -1.222e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 265

GenotypeQuality
all individuals: 636
bin: 5.75e1
variant carriers: 620

GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 92

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 191

GenotypeQuality
all individuals: 6160
bin: 2.5e0
variant carriers: 19

GenotypeQuality
all individuals: 991
bin: 6.75e1
variant carriers: 204

GenotypeQuality
all individuals: 15039
bin: 7.5e0
variant carriers: 684

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 404

GenotypeQuality
all individuals: 567
bin: 8.75e1
variant carriers: 521

GenotypeQuality
all individuals: 9393
bin: 9.75e1
variant carriers: 9034

GenotypeQuality
all individuals: 1027
bin: 2.75e1
variant carriers: 680

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 84

Other
type: Population
allele count: 82
allele frequency: 3.474576271186441e-1
allele num: 236
num of homozygotes: 15

South Asian
type: Population
allele count: 2577
allele frequency: 3.010514018691589e-1
allele num: 8560
num of homozygotes: 408

African
type: Population
allele count: 1524
allele frequency: 4.618181818181818e-1
allele num: 3300
num of homozygotes: 298

Latino
type: Population
allele count: 447
allele frequency: 4.162011173184357e-1
allele num: 1074
num of homozygotes: 61

East Asian
type: Population
allele count: 468
allele frequency: 3.91304347826087e-1
allele num: 1196
num of homozygotes: 67

European (Non-Finnish)
type: Population
allele count: 3689
allele frequency: 2.901525876986e-1
allele num: 12714
num of homozygotes: 410

European (Finnish)
type: Population
allele count: 189
allele frequency: 3.448905109489051e-1
allele num: 548
num of homozygotes: 12

DP
type: SiteQuality
SIO_000300: 8.38326e5

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.55e-2

QD
type: SiteQuality
SIO_000300: 1.705e1

GenotypeQuality
all individuals: 381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19305
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3893
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5584
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.957e-1

DP
type: SiteQuality
SIO_000300: 7.24382e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.73e-2

QD
type: SiteQuality
SIO_000300: 3.307e1

GenotypeQuality
all individuals: 3461
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3945
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3812
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1046
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.866582756450598e-5
allele num: 12712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.79e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.893e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.27802e5

VQSLOD
type: SiteQuality
SIO_000300: -1.819e0

GenotypeQuality
all individuals: 5602
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3921
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.703577512776831e-3
allele num: 1174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.78e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 7.33071e5

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.730380939561179e-5
allele num: 14858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.616e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

DP
type: SiteQuality
SIO_000300: 7.87634e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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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: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.641870350690754e-5
allele num: 15056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 2.189381499726327e-3
allele num: 3654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.237e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

DP
type: SiteQuality
SIO_000300: 7.93134e5

FS
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e-1

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 1992
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4534
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 195
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GenotypeQuality
all individuals: 3816
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.273525721455458e-5
allele num: 15940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 966
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.182e1

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 8.13367e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.58e-1

FS
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.44e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.985e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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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
all individuals: 197
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variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.142506142506142e-5
allele num: 16280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1004
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

DP
type: SiteQuality
SIO_000300: 8.22128e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1961
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
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variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 420
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.228501228501228e-4
allele num: 16280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

QD
type: SiteQuality
SIO_000300: 8.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

DP
type: SiteQuality
SIO_000300: 8.22128e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1643
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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: 197
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GenotypeQuality
all individuals: 167
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3862
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.12082492714638e-4
allele num: 8922
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.277e0

DP
type: SiteQuality
SIO_000300: 8.29475e5

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

QD
type: SiteQuality
SIO_000300: 1.044e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.459e0

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
all individuals: 167
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GenotypeQuality
all individuals: 212
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GenotypeQuality
all individuals: 5199
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1914
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4086
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.467468562055768e-5
allele num: 18290
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

DP
type: SiteQuality
SIO_000300: 8.56813e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.819e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1