http://identifiers.org/exac.variant/18-34324084-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324084
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324084
    reference: chr 18
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3444C>A
  hgvsp: ENST00000257209.4:c.3444C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2725C>A
  hgvsp: ENST00000592930.1:c.2725C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1032C>A
  hgvsp: ENST00000591635.1:c.1032C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3330C>A
  hgvsp: ENST00000445677.1:c.3330C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3393C>A
  hgvsp: ENST00000359247.4:c.3393C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.3969C>A
  hgvsp: ENST00000590592.1:c.3969C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.494C>A
  hgvsp: ENST00000585579.1:c.494C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.381C>A
  hgvsp: ENST00000592128.1:c.381C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  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: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr1148Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

18-34324091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324091
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324091
    reference: chr 18
allele count: 41427
allele frequency: 3.415307754455968e-1
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1039G>A
  hgvsp: ENSP00000467195.1:p.Val347Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3400G>A
  hgvsp: ENSP00000352186.3:p.Val1134Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3451G>A
  hgvsp: ENSP00000257209.3:p.Val1151Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2732G>A
  hgvsp: ENSP00000468163.1:p.Val912Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.3976G>A
  hgvsp: ENSP00000466937.1:p.Val1326Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.501G>A
  hgvsp: ENSP00000465843.1:p.Val168Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3337G>A
  hgvsp: ENSP00000411430.1:p.Val1113Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.388G>A
  hgvsp: ENSP00000467462.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.25e1
  variant carriers: 667
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 8.25e1
  variant carriers: 2616
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 3.75e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 3.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 5.75e1
  variant carriers: 974
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 4.25e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 7497
  bin: 2.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.75e1
  variant carriers: 2441
genotype depth: GenotypeDepth
  all individuals: 15411
  bin: 9.75e1
  variant carriers: 15115
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 1379
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 8.75e1
  variant carriers: 2764
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 2152
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 1715
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 9.25e1
  variant carriers: 2704
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 376
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9060
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val1151Ile
num of homozygotes: 7409
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

18-34324092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324092
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324092
    reference: chr 18
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1040T>C
  hgvsp: ENSP00000467195.1:p.Val347Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.3977T>C
  hgvsp: ENSP00000466937.1:p.Val1326Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3338T>C
  hgvsp: ENSP00000411430.1:p.Val1113Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.502T>C
  hgvsp: ENSP00000465843.1:p.Val168Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3452T>C
  hgvsp: ENSP00000257209.3:p.Val1151Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.389T>C
  hgvsp: ENSP00000467462.1:p.Val130Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3401T>C
  hgvsp: ENSP00000352186.3:p.Val1134Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2733T>C
  hgvsp: ENSP00000468163.1:p.Val912Ala
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val1151Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

18-34324114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324114
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324114
    reference: chr 18
allele count: 13
allele frequency: 1.071369704961266e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2755C>T
  hgvsp: ENST00000592930.1:c.2755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.3999C>T
  hgvsp: ENST00000590592.1:c.3999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.411C>T
  hgvsp: ENST00000592128.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3474C>T
  hgvsp: ENST00000257209.4:c.3474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3360C>T
  hgvsp: ENST00000445677.1:c.3360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3423C>T
  hgvsp: ENST00000359247.4:c.3423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1062C>T
  hgvsp: ENST00000591635.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.524C>T
  hgvsp: ENST00000585579.1:c.524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1158Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

18-34324120-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324120
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324120
    reference: chr 18
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.530G>C
  hgvsp: ENST00000585579.1:c.530G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3429G>C
  hgvsp: ENST00000359247.4:c.3429G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2761G>C
  hgvsp: ENST00000592930.1:c.2761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3366G>C
  hgvsp: ENST00000445677.1:c.3366G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1068G>C
  hgvsp: ENST00000591635.1:c.1068G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3480G>C
  hgvsp: ENST00000257209.4:c.3480G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.417G>C
  hgvsp: ENST00000592128.1:c.417G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4005G>C
  hgvsp: ENST00000590592.1:c.4005G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6791
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3773
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu1160Leu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

18-34324125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324125
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324125
    reference: chr 18
allele count: 2
allele frequency: 1.648777431534517e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4010C>T
  hgvsp: ENSP00000466937.1:p.Ser1337Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1073C>T
  hgvsp: ENSP00000467195.1:p.Ser358Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3434C>T
  hgvsp: ENSP00000352186.3:p.Ser1145Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3485C>T
  hgvsp: ENSP00000257209.3:p.Ser1162Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.422C>T
  hgvsp: ENSP00000467462.1:p.Ser141Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2766C>T
  hgvsp: ENSP00000468163.1:p.Ser923Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3371C>T
  hgvsp: ENSP00000411430.1:p.Ser1124Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.535C>T
  hgvsp: ENSP00000465843.1:p.Ser179Leu
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1162Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

18-34324127-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324127
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324127
    reference: chr 18
allele count: 5
allele frequency: 4.121875618281343e-5
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3373G>C
  hgvsp: ENSP00000411430.1:p.Glu1125Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.424G>C
  hgvsp: ENSP00000467462.1:p.Glu142Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2768G>C
  hgvsp: ENSP00000468163.1:p.Glu924Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.537G>C
  hgvsp: ENSP00000465843.1:p.Glu180Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4012G>C
  hgvsp: ENSP00000466937.1:p.Glu1338Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1075G>C
  hgvsp: ENSP00000467195.1:p.Glu359Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3487G>C
  hgvsp: ENSP00000257209.3:p.Glu1163Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3436G>C
  hgvsp: ENSP00000352186.3:p.Glu1146Gln
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4370
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu1163Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

18-34324129-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324129
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324129
    reference: chr 18
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1077G>T
  hgvsp: ENSP00000467195.1:p.Glu359Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4014G>T
  hgvsp: ENSP00000466937.1:p.Glu1338Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2770G>T
  hgvsp: ENSP00000468163.1:p.Glu924Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3438G>T
  hgvsp: ENSP00000352186.3:p.Glu1146Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3375G>T
  hgvsp: ENSP00000411430.1:p.Glu1125Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3489G>T
  hgvsp: ENSP00000257209.3:p.Glu1163Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.539G>T
  hgvsp: ENSP00000465843.1:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.426G>T
  hgvsp: ENSP00000467462.1:p.Glu142Asp
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20638
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu1163Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-34324132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324132
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324132
    reference: chr 18
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3378C>T
  hgvsp: ENST00000445677.1:c.3378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2773C>T
  hgvsp: ENST00000592930.1:c.2773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3441C>T
  hgvsp: ENST00000359247.4:c.3441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1080C>T
  hgvsp: ENST00000591635.1:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4017C>T
  hgvsp: ENST00000590592.1:c.4017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.429C>T
  hgvsp: ENST00000592128.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3492C>T
  hgvsp: ENST00000257209.4:c.3492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.542C>T
  hgvsp: ENST00000585579.1:c.542C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8784
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile1164Ile
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

18-34324133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324133
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324133
    reference: chr 18
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.430G>A
  hgvsp: ENSP00000467462.1:p.Gly144Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4018G>A
  hgvsp: ENSP00000466937.1:p.Gly1340Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3493G>A
  hgvsp: ENSP00000257209.3:p.Gly1165Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1081G>A
  hgvsp: ENSP00000467195.1:p.Gly361Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3379G>A
  hgvsp: ENSP00000411430.1:p.Gly1127Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2774G>A
  hgvsp: ENSP00000468163.1:p.Gly926Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3442G>A
  hgvsp: ENSP00000352186.3:p.Gly1148Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.543G>A
  hgvsp: ENSP00000465843.1:p.Gly182Arg
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20632
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly1165Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

18-34324135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324135
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324135
    reference: chr 18
allele count: 2
allele frequency: 1.649294102124291e-5
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.545G>A
  hgvsp: ENST00000585579.1:c.545G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1083G>A
  hgvsp: ENST00000591635.1:c.1083G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2776G>A
  hgvsp: ENST00000592930.1:c.2776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3381G>A
  hgvsp: ENST00000445677.1:c.3381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3495G>A
  hgvsp: ENST00000257209.4:c.3495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4020G>A
  hgvsp: ENST00000590592.1:c.4020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3444G>A
  hgvsp: ENST00000359247.4:c.3444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.432G>A
  hgvsp: ENST00000592128.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14710
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4366
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly1165Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

18-34324144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324144
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324144
    reference: chr 18
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4029C>T
  hgvsp: ENST00000590592.1:c.4029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1092C>T
  hgvsp: ENST00000591635.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3453C>T
  hgvsp: ENST00000359247.4:c.3453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3504C>T
  hgvsp: ENST00000257209.4:c.3504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2785C>T
  hgvsp: ENST00000592930.1:c.2785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.441C>T
  hgvsp: ENST00000592128.1:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3390C>T
  hgvsp: ENST00000445677.1:c.3390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.554C>T
  hgvsp: ENST00000585579.1:c.554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20620
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr1168Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

18-34324148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324148
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324148
    reference: chr 18
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.445T>C
  hgvsp: ENSP00000467462.1:p.Ser149Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4033T>C
  hgvsp: ENSP00000466937.1:p.Ser1345Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2789T>C
  hgvsp: ENSP00000468163.1:p.Ser931Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3508T>C
  hgvsp: ENSP00000257209.3:p.Ser1170Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1096T>C
  hgvsp: ENSP00000467195.1:p.Ser366Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3457T>C
  hgvsp: ENSP00000352186.3:p.Ser1153Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.558T>C
  hgvsp: ENSP00000465843.1:p.Ser187Pro
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3394T>C
  hgvsp: ENSP00000411430.1:p.Ser1132Pro
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3761
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser1170Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

18-34324170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324170
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324170
    reference: chr 18
allele count: 13
allele frequency: 1.075002067311668e-4
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+14C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+14C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11040
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-34324171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324171
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324171
    reference: chr 18
allele count: 2
allele frequency: 1.65404082172748e-5
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+15G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10614
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

18-34324182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324182
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324182
    reference: chr 18
allele count: 21
allele frequency: 1.738612090805226e-4
allele num: 120786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+26G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+26G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9717
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

18-34324188-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324188
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324188
    reference: chr 18
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+32G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+32G>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5570
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

18-34324190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324190
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324190
    reference: chr 18
allele count: 38404
allele frequency: 3.193201849203446e-1
allele num: 120268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+34C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+34C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 10169
  bin: 3.25e1
  variant carriers: 3658
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 2.25e1
  variant carriers: 2028
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 6.25e1
  variant carriers: 1267
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.25e1
  variant carriers: 4646
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 5.75e1
  variant carriers: 2085
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.75e1
  variant carriers: 752
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 2.75e1
  variant carriers: 2564
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 4.75e1
  variant carriers: 3975
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.75e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 1.75e1
  variant carriers: 1340
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 5.25e1
  variant carriers: 2994
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.75e1
  variant carriers: 4422
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.5e0
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 34526
  bin: 9.75e1
  variant carriers: 29478
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 8.25e1
  variant carriers: 275
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 4.25e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.25e1
  variant carriers: 194
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.25e1
  variant carriers: 71
num of homozygotes: 6514
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-34324192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324192
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324192
    reference: chr 18
allele count: 7
allele frequency: 5.83683543459409e-5
allele num: 119928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+36C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+36C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13716
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

18-34324193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324193
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324193
    reference: chr 18
allele count: 8
allele frequency: 6.675344614665733e-5
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+37G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+37G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14336
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4330
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

18-34324195-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324195
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324195
    reference: chr 18
allele count: 1
allele frequency: 8.342370901810295e-6
allele num: 119870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+39T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+39T>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

18-34324202-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324202
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324202
    reference: chr 18
allele count: 2
allele frequency: 1.672744304305644e-5
allele num: 119564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+46A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+46A>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

18-34324203-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324203
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324203
    reference: chr 18
allele count: 1
allele frequency: 8.373386029842748e-6
allele num: 119426
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+47C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+47C>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3154
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4850
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12786
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

18-34324203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324203
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324203
    reference: chr 18
allele count: 24
allele frequency: 2.00961264716226e-4
allele num: 119426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+47C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+47C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11733
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12786
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

18-34324204-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34324204
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34324204
    reference: chr 18
allele count: 5
allele frequency: 4.19104457595011e-5
allele num: 119302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1104+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3516+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4041+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2797+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.453+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3465+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3402+48G>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.566+48G>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11517
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2671
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

18-34326858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326858
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326858
    reference: chr 18
allele count: 1
allele frequency: 9.050920478612675e-6
allele num: 110486
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-50C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-50C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15805
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2354
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

18-34326862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326862
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326862
    reference: chr 18
allele count: 5
allele frequency: 4.514509633963559e-5
allele num: 110754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-46T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-46T>C
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

18-34326866-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326866
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326866
    reference: chr 18
allele count: 1
allele frequency: 9.03848587284658e-6
allele num: 110638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-42C>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-42C>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

18-34326866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326866
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326866
    reference: chr 18
allele count: 541
allele frequency: 4.88982085721e-3
allele num: 110638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-42C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-42C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 1.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 1.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 3.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.75e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4065
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 2.25e1
  variant carriers: 3
num of homozygotes: 11
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

18-34326867-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326867
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326867
    reference: chr 18
allele count: 6
allele frequency: 5.413012882970661e-5
allele num: 110844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-41G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-41G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17282
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3948
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

18-34326869-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326869
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326869
    reference: chr 18
allele count: 8
allele frequency: 7.210585138984029e-5
allele num: 110948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-39C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-39C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7351
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18603
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5678
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-34326870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326870
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326870
    reference: chr 18
allele count: 3
allele frequency: 2.690679486259597e-5
allele num: 111496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-38G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-38G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13850
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

18-34326876-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326876
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326876
    reference: chr 18
allele count: 1
allele frequency: 8.90805109658109e-6
allele num: 112258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-32A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-32A>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22748
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4706
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

18-34326882-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326882
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326882
    reference: chr 18
allele count: 2
allele frequency: 1.77191863349635e-5
allele num: 112872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-26T>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-26T>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP

18-34326883-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326883
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326883
    reference: chr 18
allele count: 1
allele frequency: 8.855356605210492e-6
allele num: 112926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-25G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-25G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

18-34326886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326886
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326886
    reference: chr 18
allele count: 2
allele frequency: 1.763170886522322e-5
allele num: 113432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-22G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-22G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

18-34326893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326893
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326893
    reference: chr 18
allele count: 9
allele frequency: 7.875669431901712e-5
allele num: 114276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-15C>T
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-15C>T
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16611
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6770
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

18-34326901-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326901
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326901
    reference: chr 18
allele count: 2
allele frequency: 1.723513900139605e-5
allele num: 116042
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3517-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3466-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.454-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.567-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2798-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3403-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1105-7T>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4042-7T>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: c.3517-7T>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

18-34326917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326917
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326917
    reference: chr 18
allele count: 1
allele frequency: 8.441525552497847e-6
allele num: 118462
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3526G>A
  hgvsp: ENSP00000257209.3:p.Asp1176Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3412G>A
  hgvsp: ENSP00000411430.1:p.Asp1138Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.576G>A
  hgvsp: ENSP00000465843.1:p.Asp193Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4051G>A
  hgvsp: ENSP00000466937.1:p.Asp1351Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2807G>A
  hgvsp: ENSP00000468163.1:p.Asp937Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.463G>A
  hgvsp: ENSP00000467462.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3475G>A
  hgvsp: ENSP00000352186.3:p.Asp1159Asn
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1114G>A
  hgvsp: ENSP00000467195.1:p.Asp372Asn
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp1176Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-34326917-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326917
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326917
    reference: chr 18
allele count: 1
allele frequency: 8.441525552497847e-6
allele num: 118462
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3526G>T
  hgvsp: ENSP00000257209.3:p.Asp1176Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3412G>T
  hgvsp: ENSP00000411430.1:p.Asp1138Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4051G>T
  hgvsp: ENSP00000466937.1:p.Asp1351Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1114G>T
  hgvsp: ENSP00000467195.1:p.Asp372Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3475G>T
  hgvsp: ENSP00000352186.3:p.Asp1159Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2807G>T
  hgvsp: ENSP00000468163.1:p.Asp937Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.463G>T
  hgvsp: ENSP00000467462.1:p.Asp155Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.576G>T
  hgvsp: ENSP00000465843.1:p.Asp193Tyr
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp1176Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/18-34326918-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326918
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326918
    reference: chr 18
allele count: 2
allele frequency: 1.686340640809443e-5
allele num: 118600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4052A>C
  hgvsp: ENSP00000466937.1:p.Asp1351Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2808A>C
  hgvsp: ENSP00000468163.1:p.Asp937Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3527A>C
  hgvsp: ENSP00000257209.3:p.Asp1176Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3413A>C
  hgvsp: ENSP00000411430.1:p.Asp1138Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.577A>C
  hgvsp: ENSP00000465843.1:p.Asp193Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3476A>C
  hgvsp: ENSP00000352186.3:p.Asp1159Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1115A>C
  hgvsp: ENSP00000467195.1:p.Asp372Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.464A>C
  hgvsp: ENSP00000467462.1:p.Asp155Ala
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp1176Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

18-34326921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326921
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326921
    reference: chr 18
allele count: 1
allele frequency: 8.396587626788473e-6
allele num: 119096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1118A>G
  hgvsp: ENSP00000467195.1:p.Gln373Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3530A>G
  hgvsp: ENSP00000257209.3:p.Gln1177Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2811A>G
  hgvsp: ENSP00000468163.1:p.Gln938Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3479A>G
  hgvsp: ENSP00000352186.3:p.Gln1160Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.467A>G
  hgvsp: ENSP00000467462.1:p.Gln156Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4055A>G
  hgvsp: ENSP00000466937.1:p.Gln1352Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3416A>G
  hgvsp: ENSP00000411430.1:p.Gln1139Arg
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.580A>G
  hgvsp: ENSP00000465843.1:p.Gln194Arg
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18154
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln1177Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/18-34326930-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326930
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326930
    reference: chr 18
allele count: 2
allele frequency: 1.664890783164624e-5
allele num: 120128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4064A>C
  hgvsp: ENSP00000466937.1:p.Asp1355Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2820A>C
  hgvsp: ENSP00000468163.1:p.Asp941Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3488A>C
  hgvsp: ENSP00000352186.3:p.Asp1163Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1127A>C
  hgvsp: ENSP00000467195.1:p.Asp376Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.589A>C
  hgvsp: ENSP00000465843.1:p.Asp197Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.476A>C
  hgvsp: ENSP00000467462.1:p.Asp159Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3539A>C
  hgvsp: ENSP00000257209.3:p.Asp1180Ala
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3425A>C
  hgvsp: ENSP00000411430.1:p.Asp1142Ala
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp1180Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

18-34326930-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326930
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326930
    reference: chr 18
allele count: 5
allele frequency: 4.162226957911561e-5
allele num: 120128
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3539A>T
  hgvsp: ENSP00000257209.3:p.Asp1180Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3488A>T
  hgvsp: ENSP00000352186.3:p.Asp1163Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3425A>T
  hgvsp: ENSP00000411430.1:p.Asp1142Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1127A>T
  hgvsp: ENSP00000467195.1:p.Asp376Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2820A>T
  hgvsp: ENSP00000468163.1:p.Asp941Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4064A>T
  hgvsp: ENSP00000466937.1:p.Asp1355Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.589A>T
  hgvsp: ENSP00000465843.1:p.Asp197Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.476A>T
  hgvsp: ENSP00000467462.1:p.Asp159Val
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18473
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30169
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41791
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp1180Val
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/18-34326953-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326953
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326953
    reference: chr 18
allele count: 12
allele frequency: 9.904585823236159e-5
allele num: 121156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4087A>C
  hgvsp: ENST00000590592.1:c.4087A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2843A>C
  hgvsp: ENST00000592930.1:c.2843A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.612A>C
  hgvsp: ENST00000585579.1:c.612A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3448A>C
  hgvsp: ENST00000445677.1:c.3448A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1150A>C
  hgvsp: ENST00000591635.1:c.1150A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3511A>C
  hgvsp: ENST00000359247.4:c.3511A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3562A>C
  hgvsp: ENST00000257209.4:c.3562A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.499A>C
  hgvsp: ENST00000592128.1:c.499A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1188Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

18-34326955-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326955
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326955
    reference: chr 18
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.614A>T
  hgvsp: ENSP00000465843.1:p.Arg205Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3450A>T
  hgvsp: ENSP00000411430.1:p.Arg1150Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1152A>T
  hgvsp: ENSP00000467195.1:p.Arg384Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2845A>T
  hgvsp: ENSP00000468163.1:p.Arg949Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3564A>T
  hgvsp: ENSP00000257209.3:p.Arg1188Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3513A>T
  hgvsp: ENSP00000352186.3:p.Arg1171Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4089A>T
  hgvsp: ENSP00000466937.1:p.Arg1363Ser
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.501A>T
  hgvsp: ENSP00000467462.1:p.Arg167Ser
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1188Ser
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: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

18-34326967-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326967
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326967
    reference: chr 18
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3525A>G
  hgvsp: ENST00000359247.4:c.3525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2857A>G
  hgvsp: ENST00000592930.1:c.2857A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4101A>G
  hgvsp: ENST00000590592.1:c.4101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3462A>G
  hgvsp: ENST00000445677.1:c.3462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1164A>G
  hgvsp: ENST00000591635.1:c.1164A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.626A>G
  hgvsp: ENST00000585579.1:c.626A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3576A>G
  hgvsp: ENST00000257209.4:c.3576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.513A>G
  hgvsp: ENST00000592128.1:c.513A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1192Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

18-34326970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326970
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326970
    reference: chr 18
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2860G>A
  hgvsp: ENSP00000468163.1:p.Trp954Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.516G>A
  hgvsp: ENSP00000467462.1:p.Trp172Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3528G>A
  hgvsp: ENSP00000352186.3:p.Trp1176Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3579G>A
  hgvsp: ENSP00000257209.3:p.Trp1193Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4104G>A
  hgvsp: ENSP00000466937.1:p.Trp1368Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.629G>A
  hgvsp: ENSP00000465843.1:p.Trp210Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3465G>A
  hgvsp: ENSP00000411430.1:p.Trp1155Ter
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1167G>A
  hgvsp: ENSP00000467195.1:p.Trp389Ter
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Trp1193Ter
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

18-34326971-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326971
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326971
    reference: chr 18
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.630G>T
  hgvsp: ENSP00000465843.1:p.Asp211Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3529G>T
  hgvsp: ENSP00000352186.3:p.Asp1177Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2861G>T
  hgvsp: ENSP00000468163.1:p.Asp955Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1168G>T
  hgvsp: ENSP00000467195.1:p.Asp390Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4105G>T
  hgvsp: ENSP00000466937.1:p.Asp1369Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3580G>T
  hgvsp: ENSP00000257209.3:p.Asp1194Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.517G>T
  hgvsp: ENSP00000467462.1:p.Asp173Tyr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3466G>T
  hgvsp: ENSP00000411430.1:p.Asp1156Tyr
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7253
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp1194Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

18-34326979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326979
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326979
    reference: chr 18
allele count: 6
allele frequency: 4.945272319662403e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1176C>T
  hgvsp: ENST00000591635.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.638C>T
  hgvsp: ENST00000585579.1:c.638C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3474C>T
  hgvsp: ENST00000445677.1:c.3474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3588C>T
  hgvsp: ENST00000257209.4:c.3588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3537C>T
  hgvsp: ENST00000359247.4:c.3537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4113C>T
  hgvsp: ENST00000590592.1:c.4113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.525C>T
  hgvsp: ENST00000592128.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2869C>T
  hgvsp: ENST00000592930.1:c.2869C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1196Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

18-34326982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326982
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326982
    reference: chr 18
allele count: 599
allele frequency: 4.936379219409283e-3
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1179G>A
  hgvsp: ENST00000591635.1:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2872G>A
  hgvsp: ENST00000592930.1:c.2872G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.528G>A
  hgvsp: ENST00000592128.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3591G>A
  hgvsp: ENST00000257209.4:c.3591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3540G>A
  hgvsp: ENST00000359247.4:c.3540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4116G>A
  hgvsp: ENST00000590592.1:c.4116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.641G>A
  hgvsp: ENST00000585579.1:c.641G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3477G>A
  hgvsp: ENST00000445677.1:c.3477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 30236
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 18924
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  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: 3062
  bin: 9.75e1
  variant carriers: 581
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys1197Lys
num of homozygotes: 18
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

18-34326990-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326990
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326990
    reference: chr 18
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2880C>G
  hgvsp: ENSP00000468163.1:p.Ala961Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.536C>G
  hgvsp: ENSP00000467462.1:p.Ala179Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3599C>G
  hgvsp: ENSP00000257209.3:p.Ala1200Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3548C>G
  hgvsp: ENSP00000352186.3:p.Ala1183Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1187C>G
  hgvsp: ENSP00000467195.1:p.Ala396Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3485C>G
  hgvsp: ENSP00000411430.1:p.Ala1162Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4124C>G
  hgvsp: ENSP00000466937.1:p.Ala1375Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.649C>G
  hgvsp: ENSP00000465843.1:p.Ala217Gly
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  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: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala1200Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

18-34326997-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34326997
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34326997
    reference: chr 18
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3555T>G
  hgvsp: ENSP00000352186.3:p.His1185Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1194T>G
  hgvsp: ENSP00000467195.1:p.His398Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.656T>G
  hgvsp: ENSP00000465843.1:p.His219Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.543T>G
  hgvsp: ENSP00000467462.1:p.His181Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3606T>G
  hgvsp: ENSP00000257209.3:p.His1202Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2887T>G
  hgvsp: ENSP00000468163.1:p.His963Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4131T>G
  hgvsp: ENSP00000466937.1:p.His1377Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3492T>G
  hgvsp: ENSP00000411430.1:p.His1164Gln
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  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: 2544
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His1202Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

18-34327002-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327002
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327002
    reference: chr 18
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1199T>C
  hgvsp: ENSP00000467195.1:p.Met400Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3560T>C
  hgvsp: ENSP00000352186.3:p.Met1187Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4136T>C
  hgvsp: ENSP00000466937.1:p.Met1379Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.548T>C
  hgvsp: ENSP00000467462.1:p.Met183Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.661T>C
  hgvsp: ENSP00000465843.1:p.Met221Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2892T>C
  hgvsp: ENSP00000468163.1:p.Met965Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3611T>C
  hgvsp: ENSP00000257209.3:p.Met1204Thr
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3497T>C
  hgvsp: ENSP00000411430.1:p.Met1166Thr
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met1204Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

18-34327019-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327019
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327019
    reference: chr 18
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3514C>G
  hgvsp: ENSP00000411430.1:p.Gln1172Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2909C>G
  hgvsp: ENSP00000468163.1:p.Gln971Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1216C>G
  hgvsp: ENSP00000467195.1:p.Gln406Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.565C>G
  hgvsp: ENSP00000467462.1:p.Gln189Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.678C>G
  hgvsp: ENSP00000465843.1:p.Gln227Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3577C>G
  hgvsp: ENSP00000352186.3:p.Gln1193Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3628C>G
  hgvsp: ENSP00000257209.3:p.Gln1210Glu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4153C>G
  hgvsp: ENSP00000466937.1:p.Gln1385Glu
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2597
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln1210Glu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

18-34327022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327022
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327022
    reference: chr 18
allele count: 5
allele frequency: 4.12173970389422e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.568C>T
  hgvsp: ENSP00000467462.1:p.Arg190Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3517C>T
  hgvsp: ENSP00000411430.1:p.Arg1173Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2912C>T
  hgvsp: ENSP00000468163.1:p.Arg972Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4156C>T
  hgvsp: ENSP00000466937.1:p.Arg1386Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1219C>T
  hgvsp: ENSP00000467195.1:p.Arg407Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.681C>T
  hgvsp: ENSP00000465843.1:p.Arg228Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3631C>T
  hgvsp: ENSP00000257209.3:p.Arg1211Trp
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3580C>T
  hgvsp: ENSP00000352186.3:p.Arg1194Trp
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2594
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1211Trp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-34327023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327023
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327023
    reference: chr 18
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4157G>A
  hgvsp: ENSP00000466937.1:p.Arg1386Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3581G>A
  hgvsp: ENSP00000352186.3:p.Arg1194Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2913G>A
  hgvsp: ENSP00000468163.1:p.Arg972Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1220G>A
  hgvsp: ENSP00000467195.1:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3518G>A
  hgvsp: ENSP00000411430.1:p.Arg1173Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3632G>A
  hgvsp: ENSP00000257209.3:p.Arg1211Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.682G>A
  hgvsp: ENSP00000465843.1:p.Arg228Gln
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.569G>A
  hgvsp: ENSP00000467462.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg1211Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

18-34327027-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327027
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327027
    reference: chr 18
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2917G>T
  hgvsp: ENSP00000468163.1:p.Met973Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3636G>T
  hgvsp: ENSP00000257209.3:p.Met1212Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3585G>T
  hgvsp: ENSP00000352186.3:p.Met1195Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3522G>T
  hgvsp: ENSP00000411430.1:p.Met1174Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.686G>T
  hgvsp: ENSP00000465843.1:p.Met229Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.573G>T
  hgvsp: ENSP00000467462.1:p.Met191Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1224G>T
  hgvsp: ENSP00000467195.1:p.Met408Ile
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4161G>T
  hgvsp: ENSP00000466937.1:p.Met1387Ile
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met1212Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

18-34327031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327031
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327031
    reference: chr 18
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4165G>A
  hgvsp: ENSP00000466937.1:p.Glu1389Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3589G>A
  hgvsp: ENSP00000352186.3:p.Glu1197Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3526G>A
  hgvsp: ENSP00000411430.1:p.Glu1176Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1228G>A
  hgvsp: ENSP00000467195.1:p.Glu410Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2921G>A
  hgvsp: ENSP00000468163.1:p.Glu975Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.577G>A
  hgvsp: ENSP00000467462.1:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.690G>A
  hgvsp: ENSP00000465843.1:p.Glu231Lys
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3640G>A
  hgvsp: ENSP00000257209.3:p.Glu1214Lys
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu1214Lys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

18-34327039-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327039
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327039
    reference: chr 18
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1236G>C
  hgvsp: ENST00000591635.1:c.1236G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.585G>C
  hgvsp: ENST00000592128.1:c.585G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3597G>C
  hgvsp: ENST00000359247.4:c.3597G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4173G>C
  hgvsp: ENST00000590592.1:c.4173G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2929G>C
  hgvsp: ENST00000592930.1:c.2929G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3648G>C
  hgvsp: ENST00000257209.4:c.3648G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3534G>C
  hgvsp: ENST00000445677.1:c.3534G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.698G>C
  hgvsp: ENST00000585579.1:c.698G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu1216Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

18-34327042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327042
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327042
    reference: chr 18
allele count: 2
allele frequency: 1.651254953764861e-5
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4176A>G
  hgvsp: ENST00000590592.1:c.4176A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3537A>G
  hgvsp: ENST00000445677.1:c.3537A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3600A>G
  hgvsp: ENST00000359247.4:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.701A>G
  hgvsp: ENST00000585579.1:c.701A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.588A>G
  hgvsp: ENST00000592128.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1239A>G
  hgvsp: ENST00000591635.1:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2932A>G
  hgvsp: ENST00000592930.1:c.2932A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3651A>G
  hgvsp: ENST00000257209.4:c.3651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42698
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys1217Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

18-34327053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327053
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327053
    reference: chr 18
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3548A>G
  hgvsp: ENSP00000411430.1:p.Glu1183Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2943A>G
  hgvsp: ENSP00000468163.1:p.Glu982Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4187A>G
  hgvsp: ENSP00000466937.1:p.Glu1396Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1250A>G
  hgvsp: ENSP00000467195.1:p.Glu417Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.712A>G
  hgvsp: ENSP00000465843.1:p.Glu238Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3662A>G
  hgvsp: ENSP00000257209.3:p.Glu1221Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3611A>G
  hgvsp: ENSP00000352186.3:p.Glu1204Gly
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.599A>G
  hgvsp: ENSP00000467462.1:p.Glu200Gly
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu1221Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

18-34327056-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327056
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327056
    reference: chr 18
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2946G>T
  hgvsp: ENSP00000468163.1:p.Arg983Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1253G>T
  hgvsp: ENSP00000467195.1:p.Arg418Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.602G>T
  hgvsp: ENSP00000467462.1:p.Arg201Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3551G>T
  hgvsp: ENSP00000411430.1:p.Arg1184Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4190G>T
  hgvsp: ENSP00000466937.1:p.Arg1397Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.715G>T
  hgvsp: ENSP00000465843.1:p.Arg239Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3614G>T
  hgvsp: ENSP00000352186.3:p.Arg1205Leu
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3665G>T
  hgvsp: ENSP00000257209.3:p.Arg1222Leu
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg1222Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-34327069-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327069
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327069
    reference: chr 18
allele count: 1
allele frequency: 8.34278849362611e-6
allele num: 119864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4203A>G
  hgvsp: ENST00000590592.1:c.4203A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3678A>G
  hgvsp: ENST00000257209.4:c.3678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3627A>G
  hgvsp: ENST00000359247.4:c.3627A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1266A>G
  hgvsp: ENST00000591635.1:c.1266A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2959A>G
  hgvsp: ENST00000592930.1:c.2959A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.728A>G
  hgvsp: ENST00000585579.1:c.728A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.615A>G
  hgvsp: ENST00000592128.1:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3564A>G
  hgvsp: ENST00000445677.1:c.3564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1226Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-34327073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327073
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327073
    reference: chr 18
allele count: 1
allele frequency: 8.370442294170824e-6
allele num: 119468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3631A>G
  hgvsp: ENSP00000352186.3:p.Ile1211Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4207A>G
  hgvsp: ENSP00000466937.1:p.Ile1403Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3568A>G
  hgvsp: ENSP00000411430.1:p.Ile1190Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3682A>G
  hgvsp: ENSP00000257209.3:p.Ile1228Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2963A>G
  hgvsp: ENSP00000468163.1:p.Ile989Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.732A>G
  hgvsp: ENSP00000465843.1:p.Ile245Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1270A>G
  hgvsp: ENSP00000467195.1:p.Ile424Val
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.619A>G
  hgvsp: ENSP00000467462.1:p.Ile207Val
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile1228Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

18-34327100-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327100
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327100
    reference: chr 18
allele count: 3
allele frequency: 2.568361214321182e-5
allele num: 116806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+2T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+2T>C
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38005
  bin: 6.25e1
  variant carriers: 0
hgvs: c.3707+2T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

18-34327102-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327102
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327101
    reference: chr 18
allele count: 2
allele frequency: 1.715795614426409e-5
allele num: 116564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+5delG
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+5delG
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: c.3707+5delG
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: AG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

18-34327104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327104
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327104
    reference: chr 18
allele count: 1
allele frequency: 8.58885167053165e-6
allele num: 116430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+6T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+6T>C
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
hgvs: c.3707+6T>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

18-34327108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327108
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327108
    reference: chr 18
allele count: 1
allele frequency: 8.630361612151549e-6
allele num: 115870
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+10T>C
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+10T>C
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6834
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

18-34327113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327113
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327113
    reference: chr 18
allele count: 1
allele frequency: 8.687342541916429e-6
allele num: 115110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+15G>A
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+15G>A
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

18-34327114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34327114
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34327114
    reference: chr 18
allele count: 1
allele frequency: 8.696408383337681e-6
allele num: 114990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467462
  ensembl transcript: ENST00000592128
  gene symbol: FHOD3
  hgvsc: ENST00000592128.1:c.644+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000352186
  ensembl transcript: ENST00000359247
  gene symbol: FHOD3
  hgvsc: ENST00000359247.4:c.3656+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000465843
  ensembl transcript: ENST00000585579
  gene symbol: FHOD3
  hgvsc: ENST00000585579.1:c.757+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000467195
  ensembl transcript: ENST00000591635
  gene symbol: FHOD3
  hgvsc: ENST00000591635.1:c.1295+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000466937
  ensembl transcript: ENST00000590592
  gene symbol: FHOD3
  hgvsc: ENST00000590592.1:c.4232+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000468163
  ensembl transcript: ENST00000592930
  gene symbol: FHOD3
  hgvsc: ENST00000592930.1:c.2988+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000411430
  ensembl transcript: ENST00000445677
  gene symbol: FHOD3
  hgvsc: ENST00000445677.1:c.3593+16A>G
  variant of: http://identifiers.org/hgnc/26178
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134775
  ensembl protein: ENSP00000257209
  ensembl transcript: ENST00000257209
  gene symbol: FHOD3
  hgvsc: ENST00000257209.4:c.3707+16A>G
  variant of: http://identifiers.org/hgnc/26178
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

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

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

GenotypeQuality
all individuals: 9598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4197
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37337
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1059
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.445e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

FS
type: SiteQuality
SIO_000300: 2.797e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.377e0

DP
type: SiteQuality
SIO_000300: 4.035085e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2465
bin: 7.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1738
bin: 7.25e1
variant carriers: 11

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 4012
bin: 6.75e1
variant carriers: 17

GenotypeQuality
all individuals: 38761
bin: 9.75e1
variant carriers: 33892

GenotypeQuality
all individuals: 2046
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1439
bin: 9.25e1
variant carriers: 14

GenotypeQuality
all individuals: 963
bin: 8.75e1
variant carriers: 10

East Asian
type: Population
allele count: 2599
allele frequency: 3.012984001854858e-1
allele num: 8626
num of homozygotes: 398

African
type: Population
allele count: 4309
allele frequency: 4.148055448594532e-1
allele num: 10388
num of homozygotes: 867

European (Non-Finnish)
type: Population
allele count: 20368
allele frequency: 3.054222648752399e-1
allele num: 66688
num of homozygotes: 3174

European (Finnish)
type: Population
allele count: 1751
allele frequency: 2.64821536600121e-1
allele num: 6612
num of homozygotes: 222

Latino
type: Population
allele count: 4725
allele frequency: 4.08454356846473e-1
allele num: 11568
num of homozygotes: 987

South Asian
type: Population
allele count: 7347
allele frequency: 4.450030284675954e-1
allele num: 16510
num of homozygotes: 1703

Other
type: Population
allele count: 328
allele frequency: 3.620309050772627e-1
allele num: 906
num of homozygotes: 58

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.91e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

QD
type: SiteQuality
SIO_000300: 1.856e1

DP
type: SiteQuality
SIO_000300: 4.186368e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.334e0

GenotypeQuality
all individuals: 14763
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20702
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4811
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.464781e6

QD
type: SiteQuality
SIO_000300: 1.815e1

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.23e0

FS
type: SiteQuality
SIO_000300: 6.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14772
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20687
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4801
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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: 9
allele frequency: 8.662175168431184e-4
allele num: 10390
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497885993583016e-5
allele num: 66698
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 2.497e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.201e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.027e0

DP
type: SiteQuality
SIO_000300: 2.463436e6

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 8650
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: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 6.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.989e1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

DP
type: SiteQuality
SIO_000300: 2.461926e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.74e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20657
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3068
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14714
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
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: 6614
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.363e0

QD
type: SiteQuality
SIO_000300: 2.037e1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 2.460941e6

FS
type: SiteQuality
SIO_000300: 6.12e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

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

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

GenotypeQuality
all individuals: 14736
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3777
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20642
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6772
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4793
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49940004799616e-5
allele num: 66672
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: 16506
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: 8650
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 2.460065e6

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

FS
type: SiteQuality
SIO_000300: 2.325e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.459e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

GenotypeQuality
all individuals: 4371
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4793
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 9.0e-4

QD
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DP
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10388
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 5.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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DP
type: SiteQuality
SIO_000300: 2.457735e6

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.846e1

QD
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SIO_000300: 1.25e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
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South Asian
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QD
type: SiteQuality
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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FS
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VQSLOD
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.129e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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South Asian
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Other
type: Population
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allele num: 906
num of homozygotes: 0

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

Latino
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 9.021199819576004e-5
allele num: 66510
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East Asian
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Other
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South Asian
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allele frequency: 1.837334639882411e-4
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European (Finnish)
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allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

African
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allele frequency: 2.892402622445044e-4
allele num: 10372
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Latino
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DP
type: SiteQuality
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BaseQRankSum
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QD
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 3.007428348019608e-5
allele num: 66502
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Latino
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10362
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East Asian
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Other
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Latino
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South Asian
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European (Finnish)
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allele num: 6608
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European (Non-Finnish)
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allele frequency: 1.504709741490866e-4
allele num: 66458
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16164
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.362e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 2.392696e6

QD
type: SiteQuality
SIO_000300: 3.278e1

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 24

GenotypeQuality
all individuals: 3856
bin: 6.75e1
variant carriers: 239

GenotypeQuality
all individuals: 454
bin: 4.75e1
variant carriers: 165

GenotypeQuality
all individuals: 768
bin: 2.25e1
variant carriers: 47

GenotypeQuality
all individuals: 8095
bin: 6.25e1
variant carriers: 241

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 18

GenotypeQuality
all individuals: 702
bin: 3.75e1
variant carriers: 107

GenotypeQuality
all individuals: 1798
bin: 9.25e1
variant carriers: 318

GenotypeQuality
all individuals: 2638
bin: 7.75e1
variant carriers: 241

GenotypeQuality
all individuals: 1142
bin: 8.75e1
variant carriers: 170

GenotypeQuality
all individuals: 371
bin: 5.75e1
variant carriers: 145

GenotypeQuality
all individuals: 1822
bin: 7.25e1
variant carriers: 181

East Asian
type: Population
allele count: 2583
allele frequency: 3.008385744234801e-1
allele num: 8586
num of homozygotes: 389

African
type: Population
allele count: 1758
allele frequency: 1.700851393188854e-1
allele num: 10336
num of homozygotes: 140

Other
type: Population
allele count: 316
allele frequency: 3.534675615212528e-1
allele num: 894
num of homozygotes: 55

European (Finnish)
type: Population
allele count: 1746
allele frequency: 2.651078044336471e-1
allele num: 6586
num of homozygotes: 219

Latino
type: Population
allele count: 4572
allele frequency: 3.974960876369327e-1
allele num: 11502
num of homozygotes: 924

European (Non-Finnish)
type: Population
allele count: 20205
allele frequency: 3.050455945407332e-1
allele num: 66236
num of homozygotes: 3119

South Asian
type: Population
allele count: 7224
allele frequency: 4.479166666666667e-1
allele num: 16128
num of homozygotes: 1668

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.18e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.48e-2

QD
type: SiteQuality
SIO_000300: 1.761e1

DP
type: SiteQuality
SIO_000300: 2.356858e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

GenotypeQuality
all individuals: 993
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7789
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9677
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 242
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.936108422071636e-4
allele num: 10330
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.358896095637798e-5
allele num: 15726
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.041565973900435e-5
allele num: 66208
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

DP
type: SiteQuality
SIO_000300: 2.015243e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9658
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 7675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16996
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5098
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022152376922845e-5
allele num: 66178
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.949270326615705e-4
allele num: 8634
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15688
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: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.008824e6

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

FS
type: SiteQuality
SIO_000300: 3.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.228e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.683e1

GenotypeQuality
all individuals: 9650
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 977
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
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: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510756586898719e-5
allele num: 66192
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.181e1

MQRankSum
type: SiteQuality
SIO_000300: -1.184e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 2.017e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.995974e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9636
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4888
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.288493750805309e-4
allele num: 15522
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e0

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.407e-1

QD
type: SiteQuality
SIO_000300: 1.871e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.374e0

DP
type: SiteQuality
SIO_000300: 1.966919e6

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4225
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.484243288808196e-5
allele num: 15422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66076
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 1.963616e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

GenotypeQuality
all individuals: 3154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4225
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9643
bin: 9.75e1
variant carriers: 23

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15422
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 2.134264648816453e-3
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513408801985592e-5
allele num: 66076
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 1.419e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

FS
type: SiteQuality
SIO_000300: 8.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 1.963616e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-2

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9624
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2840
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 2.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515794579518584e-5
allele num: 65972
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.591009198082653e-4
allele num: 15438
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.341e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.87e-2

FS
type: SiteQuality
SIO_000300: 5.97e0

DP
type: SiteQuality
SIO_000300: 1.959848e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

QD
type: SiteQuality
SIO_000300: 7.77e0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2597
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4148
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.147457006952067e-5
allele num: 10932
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.785e0

QD
type: SiteQuality
SIO_000300: 5.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e0

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.67e-1

DP
type: SiteQuality
SIO_000300: 1.350214e6

GenotypeQuality
all individuals: 4212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 4.538852578068265e-4
allele num: 11016
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

DP
type: SiteQuality
SIO_000300: 1.356694e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.186e1

GenotypeQuality
all individuals: 4065
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.373071e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.14e-2

QD
type: SiteQuality
SIO_000300: 1.596e1

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 744
bin: 1.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 514

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5420
bin: 6.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.069338766674095e-4
allele num: 62822
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.415458937198068e-3
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 37
allele frequency: 3.265090010589481e-3
allele num: 11332
num of homozygotes: 0

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

African
type: Population
allele count: 489
allele frequency: 4.989795918367347e-2
allele num: 9800
num of homozygotes: 11

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.373071e6

QD
type: SiteQuality
SIO_000300: 1.596e1

GenotypeQuality
all individuals: 2545
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4675
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3579
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21715
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variant carriers: 0

GenotypeQuality
all individuals: 674
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 577
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GenotypeQuality
all individuals: 2270
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variant carriers: 0

GenotypeQuality
all individuals: 660
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variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.181268689953554e-5
allele num: 62868
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.000900090009001e-5
allele num: 11110
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.61271676300578e-4
allele num: 8304
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

DP
type: SiteQuality
SIO_000300: 1.378444e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
all individuals: 3606
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
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variant carriers: 0

GenotypeQuality
all individuals: 2547
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 660
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variant carriers: 0

GenotypeQuality
all individuals: 2282
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.017132551848512e-5
allele num: 11090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.946346269985061e-5
allele num: 62922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.198465963566635e-4
allele num: 8344
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.013787510137875e-4
allele num: 9864
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 1.064e0

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

DP
type: SiteQuality
SIO_000300: 1.393304e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.627e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1969
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variant carriers: 0

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

GenotypeQuality
all individuals: 2543
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variant carriers: 3

GenotypeQuality
all individuals: 2332
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582428711586543e-5
allele num: 63194
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.758087201125176e-4
allele num: 11376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.309e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.41006e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1561
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GenotypeQuality
all individuals: 608
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573217544522056e-5
allele num: 63564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.361e0

DP
type: SiteQuality
SIO_000300: 1.447767e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.246e0

QD
type: SiteQuality
SIO_000300: 1.979e1

GenotypeQuality
all individuals: 306
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 292
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GenotypeQuality
all individuals: 172
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 693
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GenotypeQuality
all individuals: 616
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63868
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.721763085399449e-4
allele num: 11616
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.569e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

QD
type: SiteQuality
SIO_000300: 1.027e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 1.472045e6

GenotypeQuality
all individuals: 2569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 6536
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variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 614
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variant carriers: 1

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.58663918942126e-5
allele num: 11646
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.174e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.476781e6

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.452e0

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: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.924573243350536e-5
allele num: 10076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559429872438636e-5
allele num: 64126
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.547e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -4.145e-1

DP
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SIO_000300: 1.489379e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.673e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.001166861143524e-4
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.650874364380504e-5
allele num: 64504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.541e0

DP
type: SiteQuality
SIO_000300: 1.511862e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

QD
type: SiteQuality
SIO_000300: 1.171e1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13054
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.539549e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.213e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 2.187e0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518095700752976e-5
allele num: 65872
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14558
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 6.53e0

MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 1.573107e6

QD
type: SiteQuality
SIO_000300: 1.099e1

VQSLOD
type: SiteQuality
SIO_000300: -2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14558
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518095700752976e-5
allele num: 65872
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.55e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.573107e6

ReadPosRankSum
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SIO_000300: 1.91e0

BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 10346
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.365747063643813e-4
allele num: 14644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.39e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

MQRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.99e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51372952680815e-5
allele num: 66062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 4.301e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

MQ
type: SiteQuality
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ClippingRankSum
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.014863275950436e-5
allele num: 66338
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 890
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: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66338
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.184713375796178e-4
allele num: 15700
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: 11564
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.251e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.592749e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 12

European (Non-Finnish)
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allele count: 10
allele frequency: 1.500915558490679e-4
allele num: 66626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

QD
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MQ
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SIO_000300: 5.968e1

ReadPosRankSum
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SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

FS
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 1.606375e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001020346917952e-5
allele num: 66644
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.252e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 6.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

QD
type: SiteQuality
SIO_000300: 1.11e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.606177e6

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 9.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.929999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

DP
type: SiteQuality
SIO_000300: 1.607699e6

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

DP
type: SiteQuality
SIO_000300: 1.608184e6

VQSLOD
type: SiteQuality
SIO_000300: -2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.501e0

QD
type: SiteQuality
SIO_000300: 2.571e1

GenotypeQuality
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bin: 2.5e0
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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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

FS
type: SiteQuality
SIO_000300: 2.729e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.464e0

QD
type: SiteQuality
SIO_000300: 1.882e1

DP
type: SiteQuality
SIO_000300: 1.608293e6

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 2
allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.475e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.769e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.608654e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998500749625187e-5
allele num: 66700
num of homozygotes: 0

African
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allele count: 570
allele frequency: 5.482878030011543e-2
allele num: 10396
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East Asian
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Other
type: Population
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allele frequency: 1.101321585903084e-3
allele num: 908
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European (Finnish)
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allele count: 0
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Latino
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allele count: 26
allele frequency: 2.246026261230131e-3
allele num: 11576
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South Asian
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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Other
type: Population
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
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Latino
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allele frequency: 0.0e0
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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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: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42913
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -2.661e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.664e0

VQSLOD
type: SiteQuality
SIO_000300: -2.601e0

DP
type: SiteQuality
SIO_000300: 1.609552e6

QD
type: SiteQuality
SIO_000300: 9.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.609413e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.208e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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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: 709
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

DP
type: SiteQuality
SIO_000300: 1.608721e6

MQ
type: SiteQuality
SIO_000300: 5.739e1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

QD
type: SiteQuality
SIO_000300: 1.109e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7241
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498560460652591e-5
allele num: 66688
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.609002e6

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.55e-1

GenotypeQuality
all individuals: 0
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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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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.334e0

FS
type: SiteQuality
SIO_000300: 4.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.608876e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 1.634e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.952e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.608435e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.349e1

DP
type: SiteQuality
SIO_000300: 1.6082e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.853e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -1.481e0

FS
type: SiteQuality
SIO_000300: 4.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e0

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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.607305e6

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
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: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.503e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 1.2511e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.173e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 1.606413e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.384e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.46e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e0

VQSLOD
type: SiteQuality
SIO_000300: -5.083e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
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allele frequency: 0.0e0
allele num: 16206
num of homozygotes: 0

Other
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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: 8652
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.057e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
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SIO_000300: -1.837e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

DP
type: SiteQuality
SIO_000300: 1.600807e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

East Asian
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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: 66228
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.254e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

DP
type: SiteQuality
SIO_000300: 1.589497e6

VQSLOD
type: SiteQuality
SIO_000300: -1.428e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.429e0

FS
type: SiteQuality
SIO_000300: 4.508e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66122
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.583061e6

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.23e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13868
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.590103736344442e-5
allele num: 65358
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.393e1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 2
allele frequency: 3.02571860816944e-4
allele num: 6610
num of homozygotes: 0

MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
type: SiteQuality
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QD
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

Other
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QD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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Other
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European (Finnish)
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South Asian
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allele frequency: 7.448234768359899e-5
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MQ
type: SiteQuality
SIO_000300: 5.944e1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64696
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.634753397465261e-5
allele num: 13098
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.026e1

VQSLOD
type: SiteQuality
SIO_000300: -2.436e0

FS
type: SiteQuality
SIO_000300: 1.0772e1

MQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 1.508039e6