11-49175846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175846
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175846
    reference: chr 11
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1822G>A
  hgvsp: ENSP00000256999.2:p.Ala608Thr
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1223G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1777G>A
  hgvsp: ENSP00000431463.1:p.Ala593Thr
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.236G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1424G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1822G>A
  hgvsp: ENSP00000349129.3:p.Ala608Thr
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1777G>A
  hgvsp: ENSP00000344131.7:p.Ala593Thr
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.898G>A
  hgvsp: ENSP00000344086.4:p.Ala300Thr
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala608Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-49175847-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175847
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175847
    reference: chr 11
allele count: 4
allele frequency: 3.301528607745386e-5
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1222T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.235T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1821T>C
  hgvsp: ENST00000356696.3:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.897T>C
  hgvsp: ENST00000343844.4:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1423T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1821T>C
  hgvsp: ENST00000256999.2:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1776T>C
  hgvsp: ENST00000340334.7:c.1776T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1776T>C
  hgvsp: ENST00000533034.1:c.1776T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr607Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-49175863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175863
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175863
    reference: chr 11
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1407T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.881T>C
  hgvsp: ENSP00000344086.4:p.Val294Ala
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1805T>C
  hgvsp: ENSP00000349129.3:p.Val602Ala
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.219T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1805T>C
  hgvsp: ENSP00000256999.2:p.Val602Ala
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1760T>C
  hgvsp: ENSP00000431463.1:p.Val587Ala
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1760T>C
  hgvsp: ENSP00000344131.7:p.Val587Ala
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1206T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val602Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

11-49175865-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175865
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175865
    reference: chr 11
allele count: 4
allele frequency: 3.303600925008259e-5
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.879T>C
  hgvsp: ENST00000343844.4:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.217T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1758T>C
  hgvsp: ENST00000533034.1:c.1758T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1405T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1803T>C
  hgvsp: ENST00000356696.3:c.1803T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1803T>C
  hgvsp: ENST00000256999.2:c.1803T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1758T>C
  hgvsp: ENST00000340334.7:c.1758T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1204T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala601Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

11-49175868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175868
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175868
    reference: chr 11
allele count: 2
allele frequency: 1.652373634726284e-5
allele num: 121038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1755T>C
  hgvsp: ENST00000533034.1:c.1755T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.876T>C
  hgvsp: ENST00000343844.4:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1800T>C
  hgvsp: ENST00000256999.2:c.1800T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1755T>C
  hgvsp: ENST00000340334.7:c.1755T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1800T>C
  hgvsp: ENST00000356696.3:c.1800T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1402T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1201T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.214T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6146
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr600Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

11-49175873-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175873
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175873
    reference: chr 11
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1795G>A
  hgvsp: ENSP00000349129.3:p.Asp599Asn
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1750G>A
  hgvsp: ENSP00000431463.1:p.Asp584Asn
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1196G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.209G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1750G>A
  hgvsp: ENSP00000344131.7:p.Asp584Asn
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.871G>A
  hgvsp: ENSP00000344086.4:p.Asp291Asn
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1795G>A
  hgvsp: ENSP00000256999.2:p.Asp599Asn
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1397G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6142
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3230
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp599Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-49175875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175875
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175875
    reference: chr 11
allele count: 2
allele frequency: 1.653575857792476e-5
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1748G>A
  hgvsp: ENSP00000344131.7:p.Arg583Gln
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1793G>A
  hgvsp: ENSP00000349129.3:p.Arg598Gln
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.869G>A
  hgvsp: ENSP00000344086.4:p.Arg290Gln
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1395G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1194G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1748G>A
  hgvsp: ENSP00000431463.1:p.Arg583Gln
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1793G>A
  hgvsp: ENSP00000256999.2:p.Arg598Gln
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.207G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6140
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg598Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

11-49175876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175876
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175876
    reference: chr 11
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.868C>T
  hgvsp: ENSP00000344086.4:p.Arg290Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1747C>T
  hgvsp: ENSP00000344131.7:p.Arg583Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1792C>T
  hgvsp: ENSP00000349129.3:p.Arg598Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1193C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1747C>T
  hgvsp: ENSP00000431463.1:p.Arg583Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1792C>T
  hgvsp: ENSP00000256999.2:p.Arg598Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1394C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.206C>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg598Ter
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff

11-49175887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175887
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175887
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1781C>T
  hgvsp: ENSP00000349129.3:p.Pro594Leu
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1736C>T
  hgvsp: ENSP00000344131.7:p.Pro579Leu
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1736C>T
  hgvsp: ENSP00000431463.1:p.Pro579Leu
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.857C>T
  hgvsp: ENSP00000344086.4:p.Pro286Leu
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.195C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1182C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1781C>T
  hgvsp: ENSP00000256999.2:p.Pro594Leu
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1383C>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6127
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35753
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro594Leu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-49175893-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175893
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175893
    reference: chr 11
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.189T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1775T>G
  hgvsp: ENSP00000256999.2:p.Val592Gly
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1730T>G
  hgvsp: ENSP00000431463.1:p.Val577Gly
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1730T>G
  hgvsp: ENSP00000344131.7:p.Val577Gly
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1775T>G
  hgvsp: ENSP00000349129.3:p.Val592Gly
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1377T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.851T>G
  hgvsp: ENSP00000344086.4:p.Val284Gly
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1176T>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8115
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val592Gly
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

9-84249102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84249102
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 84249102
    reference: chr 9
allele count: 19
allele frequency: 3.538834047308624e-4
allele num: 53690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196781
  ensembl protein: ENSP00000391347
  ensembl transcript: ENST00000418319
  gene symbol: TLE1
  hgvsc: ENST00000418319.1:c.517G>A
  hgvsp: ENSP00000391347.1:p.Gly173Ser
  variant of: http://identifiers.org/hgnc/11837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196781
  ensembl protein: ENSP00000365646
  ensembl transcript: ENST00000376463
  gene symbol: TLE1
  hgvsc: ENST00000376463.1:c.319G>A
  hgvsp: ENSP00000365646.1:p.Gly107Ser
  variant of: http://identifiers.org/hgnc/11837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196781
  ensembl protein: ENSP00000365682
  ensembl transcript: ENST00000376499
  gene symbol: TLE1
  hgvsc: ENST00000376499.3:c.487G>A
  hgvsp: ENSP00000365682.3:p.Gly163Ser
  variant of: http://identifiers.org/hgnc/11837
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196781
  ensembl protein: ENSP00000365655
  ensembl transcript: ENST00000376472
  gene symbol: TLE1
  hgvsc: ENST00000376472.1:c.-489G>A
  variant of: http://identifiers.org/hgnc/11837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27749
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29892
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5572
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Gly163Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

11-49175903-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175903
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175903
    reference: chr 11
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1765A>G
  hgvsp: ENSP00000349129.3:p.Asn589Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1166A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1720A>G
  hgvsp: ENSP00000431463.1:p.Asn574Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.841A>G
  hgvsp: ENSP00000344086.4:p.Asn281Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.179A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1367A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1765A>G
  hgvsp: ENSP00000256999.2:p.Asn589Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1720A>G
  hgvsp: ENSP00000344131.7:p.Asn574Asp
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn589Asp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

11-49175907-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175907
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175907
    reference: chr 11
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1716A>G
  hgvsp: ENST00000340334.7:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.837A>G
  hgvsp: ENST00000343844.4:c.837A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1716A>G
  hgvsp: ENST00000533034.1:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1761A>G
  hgvsp: ENST00000256999.2:c.1761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1363A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1162A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1761A>G
  hgvsp: ENST00000356696.3:c.1761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.175A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7973
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu587Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-49175910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175910
    reference: chr 11
allele count: 1
allele frequency: 8.323622440486099e-6
allele num: 120140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1713G>A
  hgvsp: ENST00000340334.7:c.1713G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.172G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1758G>A
  hgvsp: ENST00000256999.2:c.1758G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1758G>A
  hgvsp: ENST00000356696.3:c.1758G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.834G>A
  hgvsp: ENST00000343844.4:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1713G>A
  hgvsp: ENST00000533034.1:c.1713G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1360G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1159G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7925
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6102
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Glu586Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

11-49175936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175936
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175936
    reference: chr 11
allele count: 1
allele frequency: 8.415666604951778e-6
allele num: 118826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1133C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1732C>T
  hgvsp: ENSP00000349129.3:p.Gln578Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1687C>T
  hgvsp: ENSP00000344131.7:p.Gln563Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1334C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1732C>T
  hgvsp: ENSP00000256999.2:p.Gln578Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.146C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.808C>T
  hgvsp: ENSP00000344086.4:p.Gln270Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1687C>T
  hgvsp: ENSP00000431463.1:p.Gln563Ter
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13614
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln578Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

11-49175937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175937
    reference: chr 11
allele count: 2
allele frequency: 1.683643404326963e-5
allele num: 118790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1333C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.145C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1731C>T
  hgvsp: ENST00000356696.3:c.1731C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1132C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1686C>T
  hgvsp: ENST00000533034.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1686C>T
  hgvsp: ENST00000340334.7:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.807C>T
  hgvsp: ENST00000343844.4:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1731C>T
  hgvsp: ENST00000256999.2:c.1731C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13657
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9478
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala577Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-49175963-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175963
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175963
    reference: chr 11
allele count: 4
allele frequency: 3.444119166523162e-5
allele num: 116140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1705A>G
  hgvsp: ENSP00000349129.3:p.Met569Val
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1106A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1660A>G
  hgvsp: ENSP00000431463.1:p.Met554Val
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1307A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.119A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1705A>G
  hgvsp: ENSP00000256999.2:p.Met569Val
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1660A>G
  hgvsp: ENSP00000344131.7:p.Met554Val
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.781A>G
  hgvsp: ENSP00000344086.4:p.Met261Val
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18137
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met569Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-49175967-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175967
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175967
    reference: chr 11
allele count: 2
allele frequency: 1.728668233992532e-5
allele num: 115696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1701T>C
  hgvsp: ENST00000356696.3:c.1701T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1303T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1701T>C
  hgvsp: ENST00000256999.2:c.1701T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1656T>C
  hgvsp: ENST00000340334.7:c.1656T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.777T>C
  hgvsp: ENST00000343844.4:c.777T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1656T>C
  hgvsp: ENST00000533034.1:c.1656T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1102T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.115T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17124
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25582
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6051
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp567Asp
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-49175970-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175970
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175970
    reference: chr 11
allele count: 1
allele frequency: 8.665210911233579e-6
allele num: 115404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.112T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1698T>A
  hgvsp: ENSP00000349129.3:p.Tyr566Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1653T>A
  hgvsp: ENSP00000344131.7:p.Tyr551Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.774T>A
  hgvsp: ENSP00000344086.4:p.Tyr258Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1653T>A
  hgvsp: ENSP00000431463.1:p.Tyr551Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1099T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1698T>A
  hgvsp: ENSP00000256999.2:p.Tyr566Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1300T>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6176
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr566Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-49175976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175976
    reference: chr 11
allele count: 1
allele frequency: 8.715660298424209e-6
allele num: 114736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1294G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1647G>A
  hgvsp: ENST00000533034.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1692G>A
  hgvsp: ENST00000256999.2:c.1692G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.768G>A
  hgvsp: ENST00000343844.4:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1093G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1692G>A
  hgvsp: ENST00000356696.3:c.1692G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1647G>A
  hgvsp: ENST00000340334.7:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.106G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5456
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys564Lys
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

11-49175984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175984
    reference: chr 11
allele count: 3
allele frequency: 2.630148515719521e-5
allele num: 114062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1639G>A
  hgvsp: ENSP00000431463.1:p.Val547Met
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1684G>A
  hgvsp: ENSP00000349129.3:p.Val562Met
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1639G>A
  hgvsp: ENSP00000344131.7:p.Val547Met
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.760G>A
  hgvsp: ENSP00000344086.4:p.Val254Met
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1085G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1684G>A
  hgvsp: ENSP00000256999.2:p.Val562Met
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1286G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.98G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6046
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val562Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-49175985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175985
    reference: chr 11
allele count: 1
allele frequency: 8.784258608573437e-6
allele num: 113840
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1683G>A
  hgvsp: ENST00000256999.2:c.1683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.759G>A
  hgvsp: ENST00000343844.4:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1084G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1285G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1683G>A
  hgvsp: ENST00000356696.3:c.1683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1638G>A
  hgvsp: ENST00000533034.1:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1638G>A
  hgvsp: ENST00000340334.7:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.97G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5250
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6972
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu561Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

11-49175986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175986
    reference: chr 11
allele count: 1
allele frequency: 8.777935780621829e-6
allele num: 113922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1682T>C
  hgvsp: ENSP00000349129.3:p.Leu561Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1083T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1682T>C
  hgvsp: ENSP00000256999.2:p.Leu561Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1637T>C
  hgvsp: ENSP00000344131.7:p.Leu546Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1284T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.758T>C
  hgvsp: ENSP00000344086.4:p.Leu253Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1637T>C
  hgvsp: ENSP00000431463.1:p.Leu546Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.96T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu561Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

11-49175994-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49175994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49175994
    reference: chr 11
allele count: 1
allele frequency: 8.819742110740682e-6
allele num: 113382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1674A>T
  hgvsp: ENST00000356696.3:c.1674A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1629A>T
  hgvsp: ENST00000533034.1:c.1629A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1629A>T
  hgvsp: ENST00000340334.7:c.1629A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1674A>T
  hgvsp: ENST00000256999.2:c.1674A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.88A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1075A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.750A>T
  hgvsp: ENST00000343844.4:c.750A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1276A>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7860
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr558Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

11-49176019-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176019
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176019
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 110560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1251C>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1604C>G
  hgvsp: ENSP00000431463.1:p.Pro535Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.725C>G
  hgvsp: ENSP00000344086.4:p.Pro242Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1050C>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.63C>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1649C>G
  hgvsp: ENSP00000256999.2:p.Pro550Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1604C>G
  hgvsp: ENSP00000344131.7:p.Pro535Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1649C>G
  hgvsp: ENSP00000349129.3:p.Pro550Arg
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6059
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro550Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

11-49176021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176021
    reference: chr 11
allele count: 6
allele frequency: 5.436358364743404e-5
allele num: 110368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1647T>C
  hgvsp: ENST00000356696.3:c.1647T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1602T>C
  hgvsp: ENST00000340334.7:c.1602T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1647T>C
  hgvsp: ENST00000256999.2:c.1647T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.61T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.723T>C
  hgvsp: ENST00000343844.4:c.723T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1048T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1602T>C
  hgvsp: ENST00000533034.1:c.1602T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1249T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr549Tyr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/11-49176026-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176026
    reference: chr 11
allele count: 2
allele frequency: 1.809889234778831e-5
allele num: 110504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1597G>T
  hgvsp: ENSP00000431463.1:p.Gly533Cys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.718G>T
  hgvsp: ENSP00000344086.4:p.Gly240Cys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1597G>T
  hgvsp: ENSP00000344131.7:p.Gly533Cys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1244G>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1642G>T
  hgvsp: ENSP00000256999.2:p.Gly548Cys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.56G>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1642G>T
  hgvsp: ENSP00000349129.3:p.Gly548Cys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1043G>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly548Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-49176026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176026
    reference: chr 11
allele count: 26
allele frequency: 2.352856005212481e-4
allele num: 110504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1597G>A
  hgvsp: ENSP00000431463.1:p.Gly533Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.56G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1642G>A
  hgvsp: ENSP00000349129.3:p.Gly548Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1244G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1597G>A
  hgvsp: ENSP00000344131.7:p.Gly533Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1043G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1642G>A
  hgvsp: ENSP00000256999.2:p.Gly548Ser
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.718G>A
  hgvsp: ENSP00000344086.4:p.Gly240Ser
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Gly548Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-49176027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176027
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176027
    reference: chr 11
allele count: 2
allele frequency: 1.815541031227306e-5
allele num: 110160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1641C>T
  hgvsp: ENST00000356696.3:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.55C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1596C>T
  hgvsp: ENST00000533034.1:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1243C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.717C>T
  hgvsp: ENST00000343844.4:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1641C>T
  hgvsp: ENST00000256999.2:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1042C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1596C>T
  hgvsp: ENST00000340334.7:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser547Ser
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: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum

11-49176044-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176044
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176044
    reference: chr 11
allele count: 1
allele frequency: 9.034566250474314e-6
allele num: 110686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579G>A
  hgvsp: ENSP00000344131.7:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624G>A
  hgvsp: ENSP00000256999.2:p.Glu542Lys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579G>A
  hgvsp: ENSP00000431463.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624G>A
  hgvsp: ENSP00000349129.3:p.Glu542Lys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700G>A
  hgvsp: ENSP00000344086.4:p.Glu234Lys
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu542Lys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

11-49176050-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176050
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176050
    reference: chr 11
allele count: 3
allele frequency: 2.705969368426749e-5
allele num: 110866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-6C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-6C>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6087
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7079
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1624-6C>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-49176050-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176050
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176051
    reference: chr 11
allele count: 2
allele frequency: 1.803979578951166e-5
allele num: 110866
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-7dupT
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-7dupT
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21254
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1624-7dupT
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-49176052-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176052
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176052
    reference: chr 11
allele count: 1
allele frequency: 9.004952723998199e-6
allele num: 111050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-8T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-8T>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12090
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20055
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1624-8T>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

11-49176056-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176056
    reference: chr 11
allele count: 2
allele frequency: 1.798270064198241e-5
allele num: 111218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-12T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-12T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6090
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-49176057-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176057
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176057
    reference: chr 11
allele count: 67425
allele frequency: 5.981529781231703e-1
allele num: 112722
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-13G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-13G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10619
  bin: 2.25e1
  variant carriers: 7906
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.5e0
  variant carriers: 1778
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 1.25e1
  variant carriers: 5029
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.25e1
  variant carriers: 5898
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 511
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.75e1
  variant carriers: 1948
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.25e1
  variant carriers: 2962
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 1.75e1
  variant carriers: 7233
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 222
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 755
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.25e1
  variant carriers: 1215
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 2.75e1
  variant carriers: 6908
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 9.75e1
  variant carriers: 1783
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 349
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 3.75e1
  variant carriers: 4264
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 9.25e1
  variant carriers: 908
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 2.75e1
  variant carriers: 842
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 4.25e1
  variant carriers: 1418
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 5.75e1
  variant carriers: 1297
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 3.25e1
  variant carriers: 1712
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 3.75e1
  variant carriers: 2265
genotype quality: GenotypeQuality
  all individuals: 7445
  bin: 6.25e1
  variant carriers: 2131
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 1.25e1
  variant carriers: 382
num of homozygotes: 20715
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

11-49176058-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176058
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176058
    reference: chr 11
allele count: 6388
allele frequency: 5.591149389069776e-2
allele num: 114252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-14T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-14T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 350
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 1.75e1
  variant carriers: 303
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.25e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 3.25e1
  variant carriers: 891
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 668
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 7.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 1.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 230
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 13674
  bin: 2.75e1
  variant carriers: 846
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 3.75e1
  variant carriers: 779
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.75e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 515
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3623
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4391
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.25e1
  variant carriers: 10
num of homozygotes: 304
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-49176066-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176066
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176066
    reference: chr 11
allele count: 1
allele frequency: 8.750131251968779e-6
allele num: 114284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-22T>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-22T>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12629
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20654
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5545
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

11-49176069-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176069
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176069
    reference: chr 11
allele count: 1
allele frequency: 8.756567425569177e-6
allele num: 114200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-25A>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-25A>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4741
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4830
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

11-49176076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176076
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176076
    reference: chr 11
allele count: 1
allele frequency: 8.777627582816916e-6
allele num: 113926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-32A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10525
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

11-49176078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176078
    reference: chr 11
allele count: 1
allele frequency: 8.78780955059142e-6
allele num: 113794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-34C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-34C>T
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

11-49176089-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176089
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176089
    reference: chr 11
allele count: 2
allele frequency: 1.761804087385483e-5
allele num: 113520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-45T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-45T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6007
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13935
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6335
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

11-49176095-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176095
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176095
    reference: chr 11
allele count: 1
allele frequency: 8.880679194344783e-6
allele num: 112604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-51A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-51A>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10280
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

11-49176096-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49176096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49176096
    reference: chr 11
allele count: 1
allele frequency: 8.909638446871826e-6
allele num: 112238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-52C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-52C>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13789
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6382
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6560
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-49177066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49177066
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49177066
    reference: chr 11
allele count: 1
allele frequency: 4.355400696864111e-4
allele num: 2296
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-1022A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-1022A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-49177073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49177073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49177073
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 2314
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-1029T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-1029T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-49177119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49177119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49177119
    reference: chr 11
allele count: 7
allele frequency: 2.617801047120419e-3
allele num: 2674
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1624-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.700-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.38-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1226-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1025-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1579-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1579-1075T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1624-1075T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-49178220-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178220
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178220
    reference: chr 11
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+49T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+49T>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3833
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
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: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-49178228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178228
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178228
    reference: chr 11
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+41G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+41G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33571
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-49178231-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178231
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178231
    reference: chr 11
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+38T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+38T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3871
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9530
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

11-49178246-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178246
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178246
    reference: chr 11
allele count: 2
allele frequency: 1.65305650147122e-5
allele num: 120988
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+23A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+23A>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-49178250-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178250
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178250
    reference: chr 11
allele count: 2
allele frequency: 1.652619401751776e-5
allele num: 121020
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+19A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+19A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33572
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum

11-49178253-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178253
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178253
    reference: chr 11
allele count: 4
allele frequency: 3.305020325875004e-5
allele num: 121028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+16A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+16A>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-49178254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178254
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178254
    reference: chr 11
allele count: 5040
allele frequency: 4.163224847183215e-2
allele num: 121060
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699+15A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578+15A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 9.75e1
  variant carriers: 3881
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.75e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 6.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 6.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 6729
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 157
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 143
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

11-49178269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178269
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178269
    reference: chr 11
allele count: 2
allele frequency: 1.652237129072764e-5
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1578G>A
  hgvsp: ENSP00000344131.7:p.Trp526Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1225G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1578G>A
  hgvsp: ENSP00000431463.1:p.Trp526Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.37G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1024G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.699G>A
  hgvsp: ENSP00000344086.4:p.Trp233Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1623G>A
  hgvsp: ENSP00000256999.2:p.Trp541Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1623G>A
  hgvsp: ENSP00000349129.3:p.Trp541Ter
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3270
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp541Ter
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-49178272-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178272
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178272
    reference: chr 11
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1620T>C
  hgvsp: ENST00000256999.2:c.1620T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1575T>C
  hgvsp: ENST00000340334.7:c.1575T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1222T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1021T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.696T>C
  hgvsp: ENST00000343844.4:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1620T>C
  hgvsp: ENST00000356696.3:c.1620T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.34T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1575T>C
  hgvsp: ENST00000533034.1:c.1575T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn540Asn
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

11-49178274-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178274
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178274
    reference: chr 11
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1573A>G
  hgvsp: ENSP00000344131.7:p.Asn525Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.694A>G
  hgvsp: ENSP00000344086.4:p.Asn232Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.32A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1573A>G
  hgvsp: ENSP00000431463.1:p.Asn525Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1618A>G
  hgvsp: ENSP00000256999.2:p.Asn540Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1618A>G
  hgvsp: ENSP00000349129.3:p.Asn540Asp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1220A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1019A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn540Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

11-49178283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178283
    reference: chr 11
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1564T>C
  hgvsp: ENSP00000344131.7:p.Tyr522His
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1609T>C
  hgvsp: ENSP00000256999.2:p.Tyr537His
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1211T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.23T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.685T>C
  hgvsp: ENSP00000344086.4:p.Tyr229His
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1564T>C
  hgvsp: ENSP00000431463.1:p.Tyr522His
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1010T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1609T>C
  hgvsp: ENSP00000349129.3:p.Tyr537His
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10279
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr537His
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-49178284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178284
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178284
    reference: chr 11
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1608G>A
  hgvsp: ENST00000356696.3:c.1608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1563G>A
  hgvsp: ENST00000533034.1:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1009G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.22G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.684G>A
  hgvsp: ENST00000343844.4:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1210G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1608G>A
  hgvsp: ENST00000256999.2:c.1608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1563G>A
  hgvsp: ENST00000340334.7:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg536Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-49178285-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178285
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178285
    reference: chr 11
allele count: 2
allele frequency: 1.653548515113433e-5
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1562G>C
  hgvsp: ENSP00000431463.1:p.Arg521Pro
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1209G>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1607G>C
  hgvsp: ENSP00000349129.3:p.Arg536Pro
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1562G>C
  hgvsp: ENSP00000344131.7:p.Arg521Pro
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1008G>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.683G>C
  hgvsp: ENSP00000344086.4:p.Arg228Pro
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1607G>C
  hgvsp: ENSP00000256999.2:p.Arg536Pro
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.21G>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31767
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3360
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg536Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-49178286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178286
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178286
    reference: chr 11
allele count: 4
allele frequency: 3.306932985003059e-5
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1561C>T
  hgvsp: ENSP00000431463.1:p.Arg521Trp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1208C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.682C>T
  hgvsp: ENSP00000344086.4:p.Arg228Trp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.20C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1007C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1561C>T
  hgvsp: ENSP00000344131.7:p.Arg521Trp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1606C>T
  hgvsp: ENSP00000349129.3:p.Arg536Trp
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1606C>T
  hgvsp: ENSP00000256999.2:p.Arg536Trp
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg536Trp
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-49178291-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178291
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178291
    reference: chr 11
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.15G>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1601G>T
  hgvsp: ENSP00000349129.3:p.Arg534Ile
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1601G>T
  hgvsp: ENSP00000256999.2:p.Arg534Ile
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.677G>T
  hgvsp: ENSP00000344086.4:p.Arg226Ile
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1203G>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*1002G>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1556G>T
  hgvsp: ENSP00000431463.1:p.Arg519Ile
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1556G>T
  hgvsp: ENSP00000344131.7:p.Arg519Ile
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg534Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-49178299-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178299
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178299
    reference: chr 11
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1195T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1548T>C
  hgvsp: ENST00000340334.7:c.1548T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1548T>C
  hgvsp: ENST00000533034.1:c.1548T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*994T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.669T>C
  hgvsp: ENST00000343844.4:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1593T>C
  hgvsp: ENST00000356696.3:c.1593T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1593T>C
  hgvsp: ENST00000256999.2:c.1593T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000532018
  gene symbol: FOLH1
  hgvsc: ENST00000532018.1:n.7T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10204
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala531Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-49178311-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178311
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178311
    reference: chr 11
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1581A>G
  hgvsp: ENST00000356696.3:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1536A>G
  hgvsp: ENST00000533034.1:c.1536A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1581A>G
  hgvsp: ENST00000256999.2:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.657A>G
  hgvsp: ENST00000343844.4:c.657A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1536A>G
  hgvsp: ENST00000340334.7:c.1536A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1183A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*982A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31763
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg527Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

11-49178313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178313
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178313
    reference: chr 11
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.655C>T
  hgvsp: ENSP00000344086.4:p.Arg219Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1579C>T
  hgvsp: ENSP00000349129.3:p.Arg527Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1181C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*980C>T
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1534C>T
  hgvsp: ENSP00000344131.7:p.Arg512Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1579C>T
  hgvsp: ENSP00000256999.2:p.Arg527Ter
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1534C>T
  hgvsp: ENSP00000431463.1:p.Arg512Ter
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9778
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg527Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

11-49178313-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178313
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178313
    reference: chr 11
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1534C>A
  hgvsp: ENST00000533034.1:c.1534C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1579C>A
  hgvsp: ENST00000356696.3:c.1579C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*980C>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1534C>A
  hgvsp: ENST00000340334.7:c.1534C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1579C>A
  hgvsp: ENST00000256999.2:c.1579C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.655C>A
  hgvsp: ENST00000343844.4:c.655C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1181C>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31763
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg527Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-49178346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178346
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178346
    reference: chr 11
allele count: 2
allele frequency: 1.666250104140632e-5
allele num: 120030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1501G>A
  hgvsp: ENSP00000344131.7:p.Gly501Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1501G>A
  hgvsp: ENSP00000431463.1:p.Gly501Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1148G>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.622G>A
  hgvsp: ENSP00000344086.4:p.Gly208Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1546G>A
  hgvsp: ENSP00000349129.3:p.Gly516Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1546G>A
  hgvsp: ENSP00000256999.2:p.Gly516Arg
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*947G>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly516Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-49178364-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178364
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178364
    reference: chr 11
allele count: 6
allele frequency: 5.014374540349001e-5
allele num: 119656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.609-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*934-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1533-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1488-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1488-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1533-5A>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1135-5A>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6224
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1533-5A>C
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

11-49178379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178379
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178379
    reference: chr 11
allele count: 8
allele frequency: 6.695793367816669e-5
allele num: 119478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1488-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1488-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1533-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1533-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1135-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.609-20T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*934-20T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-49178381-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178381
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178381
    reference: chr 11
allele count: 6
allele frequency: 5.0262201149329e-5
allele num: 119374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1488-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1533-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*934-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1533-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.609-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1488-22T>C
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1135-22T>C
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

11-49178381-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178381
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178381
    reference: chr 11
allele count: 2
allele frequency: 1.675406704977633e-5
allele num: 119374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1533-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*934-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1135-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1533-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1488-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.609-22T>A
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1488-22T>A
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31758
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6358
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

11-49178383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49178383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 49178383
    reference: chr 11
allele count: 1
allele frequency: 8.365680631776201e-6
allele num: 119536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000434928
  ensembl transcript: ENST00000525826
  gene symbol: FOLH1
  hgvsc: ENST00000525826.1:c.*934-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000256999
  ensembl transcript: ENST00000256999
  gene symbol: FOLH1
  hgvsc: ENST00000256999.2:c.1533-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344086
  ensembl transcript: ENST00000343844
  gene symbol: FOLH1
  hgvsc: ENST00000343844.4:c.609-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000349129
  ensembl transcript: ENST00000356696
  gene symbol: FOLH1
  hgvsc: ENST00000356696.3:c.1533-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000431463
  ensembl transcript: ENST00000533034
  gene symbol: FOLH1
  hgvsc: ENST00000533034.1:c.1488-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl protein: ENSP00000344131
  ensembl transcript: ENST00000340334
  gene symbol: FOLH1
  hgvsc: ENST00000340334.7:c.1488-24A>G
  variant of: http://identifiers.org/hgnc/3788
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086205
  ensembl transcript: ENST00000458311
  gene symbol: FOLH1
  hgvsc: ENST00000458311.2:n.1135-24A>G
  variant of: http://identifiers.org/hgnc/3788
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31754
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

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

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8451
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 5.372e0

VQSLOD
type: SiteQuality
SIO_000300: -4.315e0

MQRankSum
type: SiteQuality
SIO_000300: -2.32e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

MQ
type: SiteQuality
SIO_000300: 3.198e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.361e0

DP
type: SiteQuality
SIO_000300: 1.995321e6

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36262
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6157
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1863
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.998620317327015e-5
allele num: 66682
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.122e1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.385e0

DP
type: SiteQuality
SIO_000300: 1.995284e6

MQ
type: SiteQuality
SIO_000300: 4.102e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.014e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

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

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1862
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8443
bin: 6.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.366e0

DP
type: SiteQuality
SIO_000300: 1.993812e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

QD
type: SiteQuality
SIO_000300: 1.073e1

VQSLOD
type: SiteQuality
SIO_000300: -3.018e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.68e-1

MQ
type: SiteQuality
SIO_000300: 3.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e0

GenotypeQuality
all individuals: 6153
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.506926179203928e-4
allele num: 11406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.477e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

MQ
type: SiteQuality
SIO_000300: 3.746e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.617e0

MQRankSum
type: SiteQuality
SIO_000300: -6.44e-1

DP
type: SiteQuality
SIO_000300: 1.993321e6

QD
type: SiteQuality
SIO_000300: 1.173e1

GenotypeQuality
all individuals: 8421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36064
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 1.037e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.68e-1

MQ
type: SiteQuality
SIO_000300: 3.821e1

DP
type: SiteQuality
SIO_000300: 1.992606e6

VQSLOD
type: SiteQuality
SIO_000300: -4.17e0

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

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35983
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.165e0

MQ
type: SiteQuality
SIO_000300: 3.248e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.101e0

DP
type: SiteQuality
SIO_000300: 1.991334e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-1

GenotypeQuality
all individuals: 3226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35972
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
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: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

MQ
type: SiteQuality
SIO_000300: 3.352e1

VQSLOD
type: SiteQuality
SIO_000300: -3.725e0

DP
type: SiteQuality
SIO_000300: 1.990628e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 4.183e0

QD
type: SiteQuality
SIO_000300: 1.16e1

GenotypeQuality
all individuals: 769
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1857
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
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: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.007e0

DP
type: SiteQuality
SIO_000300: 1.989944e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 3.148e1

FS
type: SiteQuality
SIO_000300: 7.802e0

QD
type: SiteQuality
SIO_000300: 9.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1018
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.812125484666901e-5
allele num: 11348
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: 8578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.248e0

QD
type: SiteQuality
SIO_000300: 6.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.617e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 3.499e1

DP
type: SiteQuality
SIO_000300: 1.984657e6

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
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: 0
allele frequency: 0.0e0
allele num: 66272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 1.618e0

VQSLOD
type: SiteQuality
SIO_000300: -4.399e0

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

DP
type: SiteQuality
SIO_000300: 1.976544e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQ
type: SiteQuality
SIO_000300: 2.879e1

QD
type: SiteQuality
SIO_000300: 1.067e1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 445
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 6.274915104089768e-4
allele num: 27092
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.52112676056338e-4
allele num: 5680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.064e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

FS
type: SiteQuality
SIO_000300: 1.0607e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

MQ
type: SiteQuality
SIO_000300: 5.85e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 7.24018e5

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: -6.723e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.307e0

MQ
type: SiteQuality
SIO_000300: 2.913e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.73e-1

FS
type: SiteQuality
SIO_000300: 6.49e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.962007e6

QD
type: SiteQuality
SIO_000300: 1.215e1

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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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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514508996183437e-5
allele num: 66028
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.958411e6

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 2.807e1

FS
type: SiteQuality
SIO_000300: 2.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
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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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65982
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.172607879924953e-4
allele num: 8528
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.083e1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535060788407221e-5
allele num: 65144
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 2.558e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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DP
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FS
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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
all individuals: 2694
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11122
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.220107369448512e-4
allele num: 16392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65122
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.099e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 1.913026e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 2.642e1

QD
type: SiteQuality
SIO_000300: 7.5e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.718854592785422e-4
allele num: 10756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63486
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

FS
type: SiteQuality
SIO_000300: 6.38e-1

DP
type: SiteQuality
SIO_000300: 1.797364e6

VQSLOD
type: SiteQuality
SIO_000300: -4.753e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 2.866e1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.163155563990637e-5
allele num: 63228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 2.996e0

DP
type: SiteQuality
SIO_000300: 1.77768e6

MQ
type: SiteQuality
SIO_000300: 3.045e1

VQSLOD
type: SiteQuality
SIO_000300: -5.196e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586042823156225e-5
allele num: 63050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.221e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.25e0

QD
type: SiteQuality
SIO_000300: 3.98e0

FS
type: SiteQuality
SIO_000300: 2.4173e1

DP
type: SiteQuality
SIO_000300: 1.763475e6

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQ
type: SiteQuality
SIO_000300: 2.95e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 1
allele frequency: 6.257039169065198e-5
allele num: 15982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.969e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.56e-1

QD
type: SiteQuality
SIO_000300: 7.9e0

VQSLOD
type: SiteQuality
SIO_000300: -4.48e0

MQRankSum
type: SiteQuality
SIO_000300: -1.341e0

FS
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 2.936e1

DP
type: SiteQuality
SIO_000300: 1.738099e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.816027740319784e-5
allele num: 62292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15792
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.587e0

FS
type: SiteQuality
SIO_000300: 5.122e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

MQ
type: SiteQuality
SIO_000300: 2.809e1

DP
type: SiteQuality
SIO_000300: 1.707934e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

QD
type: SiteQuality
SIO_000300: 1.058e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

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: 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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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15754
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.489466691971911e-5
allele num: 10538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.302e1

MQ
type: SiteQuality
SIO_000300: 2.809e1

DP
type: SiteQuality
SIO_000300: 1.705398e6

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

BaseQRankSum
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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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.970089730807577e-5
allele num: 10030
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.398e1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 2.834e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615508885298869e-5
allele num: 61900
num of homozygotes: 0

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

South Asian
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
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num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.157e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14704
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.01e0

DP
type: SiteQuality
SIO_000300: 1.63889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 3.601e1

FS
type: SiteQuality
SIO_000300: 2.017e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

QD
type: SiteQuality
SIO_000300: 2.835e1

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6067
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2919
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.471980074719801e-4
allele num: 8030
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60284
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

MQ
type: SiteQuality
SIO_000300: 2.898e1

VQSLOD
type: SiteQuality
SIO_000300: -7.864e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 6.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.78e-1

FS
type: SiteQuality
SIO_000300: 2.5812e1

DP
type: SiteQuality
SIO_000300: 1.638508e6

GenotypeQuality
all individuals: 1593
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 699
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60340
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.244400199104032e-4
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.008471157724889e-4
allele num: 9916
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: -3.111e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

FS
type: SiteQuality
SIO_000300: 1.0618e1

MQ
type: SiteQuality
SIO_000300: 3.436e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.07e-1

DP
type: SiteQuality
SIO_000300: 1.647995e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 25

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.314550878355983e-5
allele num: 60340
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.64963503649635e-3
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.733200597312096e-4
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.229172357279432e-3
allele num: 14644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0618e1

MQRankSum
type: SiteQuality
SIO_000300: -4.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.647995e6

MQ
type: SiteQuality
SIO_000300: 3.436e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

GenotypeQuality
all individuals: 7418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6076
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4594
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variant carriers: 0

GenotypeQuality
all individuals: 1600
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variant carriers: 0

GenotypeQuality
all individuals: 967
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2798
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variant carriers: 0

GenotypeQuality
all individuals: 1879
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variant carriers: 0

GenotypeQuality
all individuals: 1373
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variant carriers: 0

GenotypeQuality
all individuals: 798
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variant carriers: 0

GenotypeQuality
all individuals: 702
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variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.009081735620585e-4
allele num: 9910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.662289304830613e-5
allele num: 60158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.253e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

QD
type: SiteQuality
SIO_000300: 1.068e1

MQ
type: SiteQuality
SIO_000300: 3.675e1

DP
type: SiteQuality
SIO_000300: 1.65062e6

FS
type: SiteQuality
SIO_000300: 3.116e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.235e0

GenotypeQuality
all individuals: 1678
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
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variant carriers: 0

GenotypeQuality
all individuals: 779
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GenotypeQuality
all individuals: 6081
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 731
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variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.236705416769726e-4
allele num: 8086
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14704
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.118e0

MQRankSum
type: SiteQuality
SIO_000300: -1.259e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.721e0

DP
type: SiteQuality
SIO_000300: 1.674801e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQ
type: SiteQuality
SIO_000300: 4.277e1

GenotypeQuality
all individuals: 867
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
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GenotypeQuality
all individuals: 1698
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variant carriers: 1

GenotypeQuality
all individuals: 5053
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variant carriers: 0

GenotypeQuality
all individuals: 417
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.651473114017704e-5
allele num: 60552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.928268414963363e-4
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 2.108e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 7.92e0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 1.683232e6

MQ
type: SiteQuality
SIO_000300: 3.816e1

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7079
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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: 1493
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
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GenotypeQuality
all individuals: 6087
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 718
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.302946228035408e-5
allele num: 60552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 7.92e0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 2.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 3.816e1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

DP
type: SiteQuality
SIO_000300: 1.683232e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

GenotypeQuality
all individuals: 851
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 722
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variant carriers: 0

GenotypeQuality
all individuals: 1001
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variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
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: 1
allele frequency: 1.648478454386601e-5
allele num: 60662
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3295e1

MQRankSum
type: SiteQuality
SIO_000300: 3.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 4.263e1

VQSLOD
type: SiteQuality
SIO_000300: -3.917e0

QD
type: SiteQuality
SIO_000300: 6.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.685048e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.92e-1

GenotypeQuality
all individuals: 2564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.472187886279357e-4
allele num: 8090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 4.456e1

VQSLOD
type: SiteQuality
SIO_000300: -2.302e0

QD
type: SiteQuality
SIO_000300: 1.466e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 1.691498e6

FS
type: SiteQuality
SIO_000300: 4.713e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

GenotypeQuality
all individuals: 1105
bin: 2.5e0
variant carriers: 249

GenotypeQuality
all individuals: 26708
bin: 9.75e1
variant carriers: 25489

GenotypeQuality
all individuals: 2501
bin: 5.25e1
variant carriers: 2431

GenotypeQuality
all individuals: 464
bin: 7.5e0
variant carriers: 366

GenotypeQuality
all individuals: 1372
bin: 2.25e1
variant carriers: 1077

GenotypeQuality
all individuals: 866
bin: 8.75e1
variant carriers: 709

GenotypeQuality
all individuals: 709
bin: 1.75e1
variant carriers: 643

GenotypeQuality
all individuals: 1429
bin: 8.25e1
variant carriers: 1117

GenotypeQuality
all individuals: 2468
bin: 4.75e1
variant carriers: 2418

GenotypeQuality
all individuals: 1866
bin: 7.75e1
variant carriers: 1392

GenotypeQuality
all individuals: 2886
bin: 6.75e1
variant carriers: 1845

GenotypeQuality
all individuals: 1350
bin: 7.25e1
variant carriers: 984

Latino
type: Population
allele count: 7158
allele frequency: 6.792560258113494e-1
allele num: 10538
num of homozygotes: 2421

South Asian
type: Population
allele count: 8556
allele frequency: 5.629688116857481e-1
allele num: 15198
num of homozygotes: 2431

African
type: Population
allele count: 3105
allele frequency: 3.165137614678899e-1
allele num: 9810
num of homozygotes: 499

European (Non-Finnish)
type: Population
allele count: 39752
allele frequency: 6.425500274787443e-1
allele num: 61866
num of homozygotes: 12827

European (Finnish)
type: Population
allele count: 3818
allele frequency: 6.003144654088051e-1
allele num: 6360
num of homozygotes: 1122

East Asian
type: Population
allele count: 4477
allele frequency: 5.52716049382716e-1
allele num: 8100
num of homozygotes: 1229

Other
type: Population
allele count: 559
allele frequency: 6.576470588235294e-1
allele num: 850
num of homozygotes: 186

VQSLOD
type: SiteQuality
SIO_000300: -4.052e-1

FS
type: SiteQuality
SIO_000300: 9.869999999999999e0

QD
type: SiteQuality
SIO_000300: 1.572e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

DP
type: SiteQuality
SIO_000300: 2.014679e6

MQ
type: SiteQuality
SIO_000300: 3.846e1

GenotypeQuality
all individuals: 504
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2996
bin: 3.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1526
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1976
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1674
bin: 4.75e1
variant carriers: 14

GenotypeQuality
all individuals: 368
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 1267
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1134
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 10903
bin: 9.75e1
variant carriers: 5938

GenotypeQuality
all individuals: 706
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 4550
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 19163
bin: 6.25e1
variant carriers: 13

East Asian
type: Population
allele count: 553
allele frequency: 6.752136752136752e-2
allele num: 8190
num of homozygotes: 28

South Asian
type: Population
allele count: 687
allele frequency: 4.490196078431372e-2
allele num: 15300
num of homozygotes: 31

European (Finnish)
type: Population
allele count: 276
allele frequency: 4.267161410018553e-2
allele num: 6468
num of homozygotes: 9

Other
type: Population
allele count: 34
allele frequency: 3.953488372093023e-2
allele num: 860
num of homozygotes: 1

Latino
type: Population
allele count: 282
allele frequency: 2.612562534741523e-2
allele num: 10794
num of homozygotes: 11

African
type: Population
allele count: 109
allele frequency: 1.087390263367917e-2
allele num: 10024
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 4447
allele frequency: 7.102018653379329e-2
allele num: 62616
num of homozygotes: 222

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 3.801e0

VQSLOD
type: SiteQuality
SIO_000300: -3.953e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.32e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

MQ
type: SiteQuality
SIO_000300: 3.897e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

QD
type: SiteQuality
SIO_000300: 1.688e1

DP
type: SiteQuality
SIO_000300: 1.769515e6

GenotypeQuality
all individuals: 3772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
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variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
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GenotypeQuality
all individuals: 778
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variant carriers: 0

GenotypeQuality
all individuals: 1658
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variant carriers: 0

GenotypeQuality
all individuals: 1373
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variant carriers: 0

GenotypeQuality
all individuals: 575
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variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4651
bin: 3.25e1
variant carriers: 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: 10810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594489444479878e-5
allele num: 62716
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.831e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 3.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

DP
type: SiteQuality
SIO_000300: 1.647285e6

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

MQ
type: SiteQuality
SIO_000300: 4.022e1

VQSLOD
type: SiteQuality
SIO_000300: -2.913e0

GenotypeQuality
all individuals: 1339
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5544
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.558237145855194e-5
allele num: 15248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.643984e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.143e0

MQ
type: SiteQuality
SIO_000300: 4.219e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 3.43e0

VQSLOD
type: SiteQuality
SIO_000300: -3.884e0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4390
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4981
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598312182335454e-5
allele num: 62566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15196
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.191e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.605787e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.995e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.887e1

QD
type: SiteQuality
SIO_000300: 1.364e1

GenotypeQuality
all individuals: 898
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5678
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1751
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4971
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.53e-1

MQ
type: SiteQuality
SIO_000300: 3.989e1

VQSLOD
type: SiteQuality
SIO_000300: -3.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 1.2781e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e0

QD
type: SiteQuality
SIO_000300: 1.19e1

DP
type: SiteQuality
SIO_000300: 1.6059e6

GenotypeQuality
all individuals: 6333
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
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GenotypeQuality
all individuals: 1386
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3856
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.205333675235592e-5
allele num: 62396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15110
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.209e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.54e0

DP
type: SiteQuality
SIO_000300: 1.579244e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.613e1

GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6568
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variant carriers: 0

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

GenotypeQuality
all individuals: 3181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5538
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 771
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.240079365079365e-4
allele num: 8064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

DP
type: SiteQuality
SIO_000300: 1.577762e6

QD
type: SiteQuality
SIO_000300: 1.283e1

MQ
type: SiteQuality
SIO_000300: 4.198e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.022e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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East Asian
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African
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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FS
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MQRankSum
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InbreedingCoeff
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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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African
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South Asian
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European (Finnish)
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allele frequency: NaN
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Latino
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East Asian
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Other
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European (Non-Finnish)
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DP
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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African
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Other
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European (Finnish)
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MQRankSum
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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MQ
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ClippingRankSum
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SIO_000300: -6.78e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele num: 66434
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Latino
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European (Finnish)
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South Asian
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East Asian
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African
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Other
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
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DP
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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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African
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Other
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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 frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66526
num of homozygotes: 0

South Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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QD
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DP
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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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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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Latino
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Other
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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BaseQRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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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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African
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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MQ
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FS
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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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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9823
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.003121623244087e-5
allele num: 66632
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.579e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 1.152e1

DP
type: SiteQuality
SIO_000300: 2.954159e6

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34130
bin: 9.75e1
variant carriers: 4887

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

GenotypeQuality
all individuals: 3018
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3083
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 38
allele frequency: 4.185022026431718e-2
allele num: 908
num of homozygotes: 1

African
type: Population
allele count: 296
allele frequency: 2.895148669796557e-2
allele num: 10224
num of homozygotes: 5

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

European (Finnish)
type: Population
allele count: 252
allele frequency: 3.812405446293494e-2
allele num: 6610
num of homozygotes: 7

Latino
type: Population
allele count: 406
allele frequency: 3.521859819569743e-2
allele num: 11528
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 3468
allele frequency: 5.203300825206301e-2
allele num: 66650
num of homozygotes: 103

South Asian
type: Population
allele count: 580
allele frequency: 3.515577645775245e-2
allele num: 16498
num of homozygotes: 20

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e0

MQ
type: SiteQuality
SIO_000300: 3.058e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

FS
type: SiteQuality
SIO_000300: 8.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.696e0

DP
type: SiteQuality
SIO_000300: 3.332738e6

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 2067
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10474
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 31771
bin: 9.75e1
variant carriers: 2

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: 10220
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.314279102059708e-4
allele num: 8642
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.19e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 2.96e1

VQSLOD
type: SiteQuality
SIO_000300: -4.953e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 1.593e0

DP
type: SiteQuality
SIO_000300: 2.896899e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.603e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3270
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variant carriers: 0

GenotypeQuality
all individuals: 4170
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variant carriers: 0

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31770
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 2.896649e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 9.685e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e0

QD
type: SiteQuality
SIO_000300: 1.857e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -5.607e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.11e0

MQ
type: SiteQuality
SIO_000300: 3.001e1

GenotypeQuality
all individuals: 2066
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 5.43e0

MQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.896498e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.244e0

VQSLOD
type: SiteQuality
SIO_000300: -5.542e0

QD
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 3.138e1

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3363
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3303
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3268
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4106
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31768
bin: 9.75e1
variant carriers: 1

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: 10176
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

FS
type: SiteQuality
SIO_000300: 7.292e0

QD
type: SiteQuality
SIO_000300: 1.085e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 2.858e1

VQSLOD
type: SiteQuality
SIO_000300: -5.084e0

DP
type: SiteQuality
SIO_000300: 2.895002e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

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

GenotypeQuality
all individuals: 31768
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3361
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1954
bin: 8.75e1
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: 11524
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 7.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.894923e6

VQSLOD
type: SiteQuality
SIO_000300: -5.127e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

MQ
type: SiteQuality
SIO_000300: 3.039e1

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

GenotypeQuality
all individuals: 1954
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.25e1
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GenotypeQuality
all individuals: 4084
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GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
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GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
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: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003544182134919e-5
allele num: 66588
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.119e1

DP
type: SiteQuality
SIO_000300: 2.894823e6

VQSLOD
type: SiteQuality
SIO_000300: -7.193e0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 9.87e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
all individuals: 4093
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 1954
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GenotypeQuality
all individuals: 10281
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GenotypeQuality
all individuals: 3268
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GenotypeQuality
all individuals: 2047
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GenotypeQuality
all individuals: 31766
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variant carriers: 4

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 3360
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

MQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 2.899e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.894956e6

VQSLOD
type: SiteQuality
SIO_000300: -3.753e0

FS
type: SiteQuality
SIO_000300: 5.099e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 16490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
SIO_000300: 2.891855e6

FS
type: SiteQuality
SIO_000300: 8.2902e1

QD
type: SiteQuality
SIO_000300: 7.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

MQ
type: SiteQuality
SIO_000300: 2.789e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e0

VQSLOD
type: SiteQuality
SIO_000300: -3.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

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

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.922e1

VQSLOD
type: SiteQuality
SIO_000300: -5.277e0

FS
type: SiteQuality
SIO_000300: 1.0599e1

DP
type: SiteQuality
SIO_000300: 2.889264e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

QD
type: SiteQuality
SIO_000300: 7.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
all individuals: 1946
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 10011
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 2.7e1

QD
type: SiteQuality
SIO_000300: 9.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 2.882722e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

GenotypeQuality
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bin: 8.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011231894968231e-5
allele num: 66418
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.762e1

QD
type: SiteQuality
SIO_000300: 1.1e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.981e0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 2.880191e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

FS
type: SiteQuality
SIO_000300: 1.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 9.25e1
variant carriers: 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: 8618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.762e1

QD
type: SiteQuality
SIO_000300: 1.1e1

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.981e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

FS
type: SiteQuality
SIO_000300: 1.269e0

DP
type: SiteQuality
SIO_000300: 2.880191e6

GenotypeQuality
all individuals: 3282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017865765330758e-5
allele num: 66272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 2.238e1

DP
type: SiteQuality
SIO_000300: 2.855517e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.068e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.206e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31750
bin: 9.75e1
variant carriers: 6

East Asian
type: Population
allele count: 6
allele frequency: 6.981615080288574e-4
allele num: 8594
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 9.52e0

VQSLOD
type: SiteQuality
SIO_000300: -5.409e0

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

MQ
type: SiteQuality
SIO_000300: 2.419e1

DP
type: SiteQuality
SIO_000300: 2.828344e6

FS
type: SiteQuality
SIO_000300: 3.314e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-1

GenotypeQuality
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bin: 7.75e1
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: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66012
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.215239268843705e-4
allele num: 9738
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
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: 9.720000000000001e0

FS
type: SiteQuality
SIO_000300: 1.108e0

VQSLOD
type: SiteQuality
SIO_000300: -3.793e0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 2.878e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 2.822895e6

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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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1854
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
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: 6
allele frequency: 9.097525473071325e-5
allele num: 65952
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.821394e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 2.894e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.154e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.643e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
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variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 8.75e1
variant carriers: 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: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.326122354035822e-4
allele num: 8598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: -4.643e0

QD
type: SiteQuality
SIO_000300: 1.154e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 2.821394e6

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQ
type: SiteQuality
SIO_000300: 2.894e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1