14-106805241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106805241
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 106805241
    reference: chr 14
allele count: 1
allele frequency: 8.479462741240714e-6
allele num: 117932
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000231475
  ensembl protein: ENSP00000395656
  ensembl transcript: ENST00000438142
  gene symbol: IGHV4-31
  hgvsc: ENST00000438142.2:c.322G>A
  hgvsp: ENSP00000395656.2:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/5649
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46819
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala108Thr
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16114
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11408
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-61624910-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624910
    reference: chr 11
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-16T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-16T>C
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5960
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

11-61624913-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624913
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624913
    reference: chr 11
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-13C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-13C>G
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5961
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17928
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

11-61624917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624917
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624917
    reference: chr 11
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-9C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-9C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17958
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12261
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

11-61624919-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624919
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624919
    reference: chr 11
allele count: 7
allele frequency: 5.77062586559388e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-7C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-7C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17977
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12259
  bin: 9.75e1
  variant carriers: 7
hgvs: c.806-7C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ

11-61624920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624920
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624920
    reference: chr 11
allele count: 5
allele frequency: 4.121603798470061e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-6C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-6C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: c.806-6C>T
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

11-61624922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624922
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624922
    reference: chr 11
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.713-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2886-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.104-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.806-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.740-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.806-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.104-4G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.806-4G>A
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-61624933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624933
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624933
    reference: chr 11
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.111G>A
  hgvsp: ENST00000355484.3:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.813G>A
  hgvsp: ENST00000278840.4:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.813G>A
  hgvsp: ENST00000521849.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.111G>A
  hgvsp: ENST00000521571.2:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.720G>A
  hgvsp: ENST00000522056.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.747G>A
  hgvsp: ENST00000257261.6:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2893G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10437
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro271Pro
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

11-61624936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624936
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624936
    reference: chr 11
allele count: 10
allele frequency: 8.241169586787757e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.750G>A
  hgvsp: ENST00000257261.6:c.750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.114G>A
  hgvsp: ENST00000355484.3:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.816G>A
  hgvsp: ENST00000521849.1:c.816G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.723G>A
  hgvsp: ENST00000522056.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.816G>A
  hgvsp: ENST00000278840.4:c.816G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.114G>A
  hgvsp: ENST00000521571.2:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2896G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5959
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro272Pro
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

11-61624949-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624949
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624949
    reference: chr 11
allele count: 4
allele frequency: 3.295707341188102e-5
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.829A>G
  hgvsp: ENSP00000431091.1:p.Met277Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.829A>G
  hgvsp: ENSP00000278840.4:p.Met277Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2909A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.736A>G
  hgvsp: ENSP00000429500.1:p.Met246Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.127A>G
  hgvsp: ENSP00000437965.1:p.Met43Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.127A>G
  hgvsp: ENSP00000443867.1:p.Met43Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.763A>G
  hgvsp: ENSP00000257261.6:p.Met255Val
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met277Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-61624960-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624960
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624960
    reference: chr 11
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.138G>T
  hgvsp: ENSP00000437965.1:p.Gln46His
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.840G>T
  hgvsp: ENSP00000431091.1:p.Gln280His
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.840G>T
  hgvsp: ENSP00000278840.4:p.Gln280His
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2920G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.774G>T
  hgvsp: ENSP00000257261.6:p.Gln258His
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.138G>T
  hgvsp: ENSP00000443867.1:p.Gln46His
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.747G>T
  hgvsp: ENSP00000429500.1:p.Gln249His
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln280His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

11-61624972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624972
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624972
    reference: chr 11
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.150C>T
  hgvsp: ENST00000355484.3:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.852C>T
  hgvsp: ENST00000521849.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.759C>T
  hgvsp: ENST00000522056.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2932C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.150C>T
  hgvsp: ENST00000521571.2:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.852C>T
  hgvsp: ENST00000278840.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.786C>T
  hgvsp: ENST00000257261.6:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12237
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10448
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile284Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-61624982-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624982
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624982
    reference: chr 11
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.160A>T
  hgvsp: ENSP00000443867.1:p.Ile54Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.160A>T
  hgvsp: ENSP00000437965.1:p.Ile54Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.862A>T
  hgvsp: ENSP00000431091.1:p.Ile288Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.796A>T
  hgvsp: ENSP00000257261.6:p.Ile266Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.862A>T
  hgvsp: ENSP00000278840.4:p.Ile288Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.769A>T
  hgvsp: ENSP00000429500.1:p.Ile257Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2942A>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18047
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile288Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-61624984-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624984
    reference: chr 11
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.162C>A
  hgvsp: ENST00000521571.2:c.162C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.864C>A
  hgvsp: ENST00000278840.4:c.864C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.771C>A
  hgvsp: ENST00000522056.1:c.771C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.864C>A
  hgvsp: ENST00000521849.1:c.864C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.162C>A
  hgvsp: ENST00000355484.3:c.162C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.798C>A
  hgvsp: ENST00000257261.6:c.798C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2944C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5961
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile288Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-61624984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624984
    reference: chr 11
allele count: 8
allele frequency: 6.592827004219409e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.162C>T
  hgvsp: ENST00000355484.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.864C>T
  hgvsp: ENST00000278840.4:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.798C>T
  hgvsp: ENST00000257261.6:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.162C>T
  hgvsp: ENST00000521571.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.771C>T
  hgvsp: ENST00000522056.1:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.864C>T
  hgvsp: ENST00000521849.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2944C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4075
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18051
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile288Ile
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-61624985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624985
    reference: chr 11
allele count: 4
allele frequency: 3.296359171295305e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.772G>A
  hgvsp: ENSP00000429500.1:p.Val258Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.163G>A
  hgvsp: ENSP00000437965.1:p.Val55Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.799G>A
  hgvsp: ENSP00000257261.6:p.Val267Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.163G>A
  hgvsp: ENSP00000443867.1:p.Val55Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.865G>A
  hgvsp: ENSP00000431091.1:p.Val289Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.865G>A
  hgvsp: ENSP00000278840.4:p.Val289Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2945G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val289Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

11-61624986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624986
    reference: chr 11
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.164T>C
  hgvsp: ENSP00000437965.1:p.Val55Ala
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.800T>C
  hgvsp: ENSP00000257261.6:p.Val267Ala
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2946T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.866T>C
  hgvsp: ENSP00000431091.1:p.Val289Ala
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.866T>C
  hgvsp: ENSP00000278840.4:p.Val289Ala
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.164T>C
  hgvsp: ENSP00000443867.1:p.Val55Ala
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.773T>C
  hgvsp: ENSP00000429500.1:p.Val258Ala
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10436
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val289Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

11-61624996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61624996
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61624996
    reference: chr 11
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2956C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.174C>T
  hgvsp: ENST00000355484.3:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.876C>T
  hgvsp: ENST00000278840.4:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.783C>T
  hgvsp: ENST00000522056.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.810C>T
  hgvsp: ENST00000257261.6:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.174C>T
  hgvsp: ENST00000521571.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.876C>T
  hgvsp: ENST00000521849.1:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18008
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn292Asn
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

11-61625011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625011
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625011
    reference: chr 11
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+9G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+9G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17869
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4586
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

11-61625013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625013
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625013
    reference: chr 11
allele count: 3
allele frequency: 2.474675817467912e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+11G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+11G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10399
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-61625024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625024
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625024
    reference: chr 11
allele count: 2
allele frequency: 1.650737054094653e-5
allele num: 121158
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+22C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+22C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-61625040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625040
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625040
    reference: chr 11
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+38G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+38G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

11-61625044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625044
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625044
    reference: chr 11
allele count: 2
allele frequency: 1.652974527662529e-5
allele num: 120994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+42G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+42G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13651
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4431
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9589
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-61625049-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625049
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625049
    reference: chr 11
allele count: 4
allele frequency: 3.31092937787637e-5
allele num: 120812
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+47G>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+47G>C
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

11-61625053-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625053
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625052
    reference: chr 11
allele count: 22
allele frequency: 1.823456278491504e-4
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+56delG
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+56delG
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7750
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5282
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: AG
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-61625054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61625054
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61625054
    reference: chr 11
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.180+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.882+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.789+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.882+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.180+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2962+52G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.816+52G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4846
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4997
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-61630396-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630396
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630396
    reference: chr 11
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.952A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-48A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-48A>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

11-61630398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630398
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630398
    reference: chr 11
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-46G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.954G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-46G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-61630407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630407
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630407
    reference: chr 11
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-37G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.963G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-37G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-61630412-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630412
    reference: chr 11
allele count: 4
allele frequency: 3.299023489047242e-5
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.968C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-32C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-32C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-61630420-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630420
    reference: chr 11
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.976A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-24A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-24A>C
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4439
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

11-61630421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630421
    reference: chr 11
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.977C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-23C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5032
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-61630430-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630430
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630430
    reference: chr 11
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.986A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-14A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-14A>C
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4449
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-61630435-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630435
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630435
    reference: chr 11
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.991T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-9T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-9T>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9803
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-61630436-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630436
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630436
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.992C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-8C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-8C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
hgvs: c.883-8C>A
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-61630439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630439
    reference: chr 11
allele count: 8
allele frequency: 6.591740549091988e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.995C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-5C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-5C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: c.883-5C>T
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ

11-61630440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630440
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630440
    reference: chr 11
allele count: 7
allele frequency: 5.767772980455489e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.817-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.883-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.181-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.790-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.883-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2963-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.181-4G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.996G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9936
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5079
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4452
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: c.883-4G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-61630452-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630452
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630452
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.891C>T
  hgvsp: ENST00000278840.4:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2971C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1008C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.798C>T
  hgvsp: ENST00000522056.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.189C>T
  hgvsp: ENST00000355484.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.825C>T
  hgvsp: ENST00000257261.6:c.825C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.189C>T
  hgvsp: ENST00000521571.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.891C>T
  hgvsp: ENST00000521849.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala297Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-61630458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630458
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630458
    reference: chr 11
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1014C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.897C>T
  hgvsp: ENST00000521849.1:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.195C>T
  hgvsp: ENST00000355484.3:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.831C>T
  hgvsp: ENST00000257261.6:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.897C>T
  hgvsp: ENST00000278840.4:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.195C>T
  hgvsp: ENST00000521571.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2977C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.804C>T
  hgvsp: ENST00000522056.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala299Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

11-61630459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630459
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630459
    reference: chr 11
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.196G>A
  hgvsp: ENSP00000437965.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.898G>A
  hgvsp: ENSP00000431091.1:p.Val300Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1015G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.805G>A
  hgvsp: ENSP00000429500.1:p.Val269Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.898G>A
  hgvsp: ENSP00000278840.4:p.Val300Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2978G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.196G>A
  hgvsp: ENSP00000443867.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.832G>A
  hgvsp: ENSP00000257261.6:p.Val278Ile
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27726
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val300Ile
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-61630468-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630468
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630468
    reference: chr 11
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.841T>A
  hgvsp: ENSP00000257261.6:p.Tyr281Asn
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.205T>A
  hgvsp: ENSP00000437965.1:p.Tyr69Asn
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.907T>A
  hgvsp: ENSP00000278840.4:p.Tyr303Asn
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1024T>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.205T>A
  hgvsp: ENSP00000443867.1:p.Tyr69Asn
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2987T>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.814T>A
  hgvsp: ENSP00000429500.1:p.Tyr272Asn
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.907T>A
  hgvsp: ENSP00000431091.1:p.Tyr303Asn
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4039
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr303Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

11-61630471-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630471
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630471
    reference: chr 11
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.910A>G
  hgvsp: ENSP00000278840.4:p.Ile304Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.208A>G
  hgvsp: ENSP00000437965.1:p.Ile70Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.844A>G
  hgvsp: ENSP00000257261.6:p.Ile282Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.910A>G
  hgvsp: ENSP00000431091.1:p.Ile304Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.208A>G
  hgvsp: ENSP00000443867.1:p.Ile70Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.2990A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1027A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.817A>G
  hgvsp: ENSP00000429500.1:p.Ile273Val
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4457
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile304Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-61630492-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630492
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630492
    reference: chr 11
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3011A>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.229A>C
  hgvsp: ENSP00000443867.1:p.Ile77Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.931A>C
  hgvsp: ENSP00000278840.4:p.Ile311Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.931A>C
  hgvsp: ENSP00000431091.1:p.Ile311Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.865A>C
  hgvsp: ENSP00000257261.6:p.Ile289Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.838A>C
  hgvsp: ENSP00000429500.1:p.Ile280Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.229A>C
  hgvsp: ENSP00000437965.1:p.Ile77Leu
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1048A>C
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9864
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile311Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

11-61630503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630503
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630503
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.240C>T
  hgvsp: ENST00000521571.2:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.942C>T
  hgvsp: ENST00000278840.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.849C>T
  hgvsp: ENST00000522056.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1059C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.942C>T
  hgvsp: ENST00000521849.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.240C>T
  hgvsp: ENST00000355484.3:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.876C>T
  hgvsp: ENST00000257261.6:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3022C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr314Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

11-61630518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630518
    reference: chr 11
allele count: 12
allele frequency: 9.884515905833511e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.255C>T
  hgvsp: ENST00000355484.3:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1074C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3037C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.864C>T
  hgvsp: ENST00000522056.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.891C>T
  hgvsp: ENST00000257261.6:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.957C>T
  hgvsp: ENST00000521849.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.957C>T
  hgvsp: ENST00000278840.4:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.255C>T
  hgvsp: ENST00000521571.2:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala319Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-61630522-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630522
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630522
    reference: chr 11
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.259C>G
  hgvsp: ENSP00000437965.1:p.Leu87Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.868C>G
  hgvsp: ENSP00000429500.1:p.Leu290Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.961C>G
  hgvsp: ENSP00000431091.1:p.Leu321Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3041C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1078C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.961C>G
  hgvsp: ENSP00000278840.4:p.Leu321Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.895C>G
  hgvsp: ENSP00000257261.6:p.Leu299Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.259C>G
  hgvsp: ENSP00000443867.1:p.Leu87Val
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu321Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-61630537-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630537
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630537
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.274A>G
  hgvsp: ENSP00000443867.1:p.Ile92Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.910A>G
  hgvsp: ENSP00000257261.6:p.Ile304Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1093A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.883A>G
  hgvsp: ENSP00000429500.1:p.Ile295Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.976A>G
  hgvsp: ENSP00000431091.1:p.Ile326Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.976A>G
  hgvsp: ENSP00000278840.4:p.Ile326Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.274A>G
  hgvsp: ENSP00000437965.1:p.Ile92Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3056A>G
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile326Val
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

11-61630544-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630544
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630544
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+3G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+3G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+3G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000443867
  ensembl transcript: ENST00000521571
  gene symbol: FADS2
  hgvsc: ENST00000521571.2:c.281G>T
  hgvsp: ENSP00000443867.1:p.Cys94Phe
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1100G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+3G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+3G>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+3G>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys94Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-61630556-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630556
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630556
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+15C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+15C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+15C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+15C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+15C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1112C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+15C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9735
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-61630560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630560
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630560
    reference: chr 11
allele count: 16
allele frequency: 1.318934960019784e-4
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+19T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+19T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+19T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+19T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1116T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+19T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+19T>C
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5043
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-61630561-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630561
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630561
    reference: chr 11
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+20T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+20T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+20T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+20T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1117T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+20T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+20T>C
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4043
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4456
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-61630565-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630565
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630565
    reference: chr 11
allele count: 16
allele frequency: 1.319652931279074e-4
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+24C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1121C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+24C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+24C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+24C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+24C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+24C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4039
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27712
  bin: 9.75e1
  variant carriers: 16
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-61630574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630574
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630574
    reference: chr 11
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+33C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+33C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+33C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1130C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+33C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+33C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+33C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4429
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4894
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-61630583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630583
    reference: chr 11
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1139C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+42C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+42C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+42C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+42C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+42C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+42C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8529
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4358
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-61630584-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630584
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630584
    reference: chr 11
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+43A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+43A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+43A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+43A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1140A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+43A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+43A>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2603
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-61630595-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630595
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630595
    reference: chr 11
allele count: 74
allele frequency: 6.124813772554212e-4
allele num: 120820
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+54C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+54C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1151C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+54C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+54C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+54C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+54C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6325
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4329
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

11-61630597-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630597
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630597
    reference: chr 11
allele count: 2
allele frequency: 1.655409879486161e-5
allele num: 120816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+56T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+56T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+56T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+56T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+56T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1153T>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+56T>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4291
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-61630598-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630598
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630598
    reference: chr 11
allele count: 1
allele frequency: 8.27841981522567e-6
allele num: 120796
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.914+57T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.980+57T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3060+57T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1154T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.278+57T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.980+57T>C
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.887+57T>C
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27649
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-61630704-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630704
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630704
    reference: chr 11
allele count: 2
allele frequency: 1.66725020423815e-5
allele num: 119958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-50C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-50C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1260C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-50C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-50C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-50C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-50C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

11-61630706-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630706
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630706
    reference: chr 11
allele count: 1
allele frequency: 8.333611120370679e-6
allele num: 119996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1262G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-48G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-48G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-48G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-48G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-48G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-48G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22774
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-61630715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630715
    reference: chr 11
allele count: 19
allele frequency: 1.6e-4
allele num: 118750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-39C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-39C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-39C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1271C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-39C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-39C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-39C>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11363
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19593
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-61630718-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630718
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630718
    reference: chr 11
allele count: 1
allele frequency: 8.323206765102459e-6
allele num: 120146
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-36C>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1274C>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD

11-61630719-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630719
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630719
    reference: chr 11
allele count: 2
allele frequency: 1.665778251599147e-5
allele num: 120064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1275C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-35C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-35C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-35C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-35C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-35C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-35C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

11-61630720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630720
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630720
    reference: chr 11
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-34G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-34G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-34G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-34G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-34G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1276G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-34G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5015
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

11-61630725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630725
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630725
    reference: chr 11
allele count: 8
allele frequency: 6.649378283130527e-5
allele num: 120312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1281C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-29C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-29C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-29C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-29C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-29C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-29C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5021
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

11-61630728-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630728
    reference: chr 11
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-26C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-26C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-26C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-26C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-26C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1284C>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-26C>G
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29716
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-61630728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630728
    reference: chr 11
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1284C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-26C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-26C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-26C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-26C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-26C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-26C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-61630731-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630731
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630731
    reference: chr 11
allele count: 6
allele frequency: 4.976032111993896e-5
allele num: 120578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1287C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-23C>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-23C>T
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12059
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-61630732-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630732
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630732
    reference: chr 11
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1288G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-22G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-22G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-22G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-22G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-22G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-22G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-61630740-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630740
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630740
    reference: chr 11
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3061-14G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.981-14G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.888-14G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.915-14G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1296G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.981-14G>A
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.279-14G>A
  variant of: http://identifiers.org/hgnc/3575
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-61630795-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630795
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630795
    reference: chr 11
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.956A>T
  hgvsp: ENSP00000257261.6:p.Asn319Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.320A>T
  hgvsp: ENSP00000437965.1:p.Asn107Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.1022A>T
  hgvsp: ENSP00000278840.4:p.Asn341Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1351A>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.1022A>T
  hgvsp: ENSP00000431091.1:p.Asn341Ile
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3102A>T
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.929A>T
  hgvsp: ENSP00000429500.1:p.Asn310Ile
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5012
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn341Ile
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-61630800-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 61630800
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 61630800
    reference: chr 11
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000257261
  ensembl transcript: ENST00000257261
  gene symbol: FADS2
  hgvsc: ENST00000257261.6:c.961A>G
  hgvsp: ENSP00000257261.6:p.Ile321Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000429500
  ensembl transcript: ENST00000522056
  gene symbol: FADS2
  hgvsc: ENST00000522056.1:c.934A>G
  hgvsp: ENSP00000429500.1:p.Ile312Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000437965
  ensembl transcript: ENST00000355484
  gene symbol: FADS2
  hgvsc: ENST00000355484.3:c.325A>G
  hgvsp: ENSP00000437965.1:p.Ile109Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000522359
  gene symbol: FADS2
  hgvsc: ENST00000522359.2:n.1356A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000431091
  ensembl transcript: ENST00000521849
  gene symbol: FADS2
  hgvsc: ENST00000521849.1:c.1027A>G
  hgvsp: ENSP00000431091.1:p.Ile343Val
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134824
  ensembl transcript: ENST00000523235
  gene symbol: FADS2
  hgvsc: ENST00000523235.1:n.3107A>G
  variant of: http://identifiers.org/hgnc/3575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134824
  ensembl protein: ENSP00000278840
  ensembl transcript: ENST00000278840
  gene symbol: FADS2
  hgvsc: ENST00000278840.4:c.1027A>G
  hgvsp: ENSP00000278840.4:p.Ile343Val
  variant of: http://identifiers.org/hgnc/3575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile343Val
num of homozygotes: 0
reference allele: A

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519895431194334e-5
allele num: 65794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.953e0

MQ
type: SiteQuality
SIO_000300: 5.654e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.302e0

FS
type: SiteQuality
SIO_000300: 8.092000000000001e0

QD
type: SiteQuality
SIO_000300: 3.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.3031036e7

BaseQRankSum
type: SiteQuality
SIO_000300: -5.178e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

GenotypeQuality
all individuals: 17910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4066
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12267
bin: 9.75e1
variant carriers: 2

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

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

FS
type: SiteQuality
SIO_000300: 6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.641e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.1e1

DP
type: SiteQuality
SIO_000300: 2.342395e6

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12257
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 4592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.596e1

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000660145231951e-5
allele num: 66652
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.037e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.287e0

DP
type: SiteQuality
SIO_000300: 2.342614e6

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

African
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allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.501650363079878e-5
allele num: 66652
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.342813e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

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

African
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allele count: 5
allele frequency: 4.809542131589073e-4
allele num: 10396
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.673e0

DP
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SIO_000300: 2.342928e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

QD
type: SiteQuality
SIO_000300: 1.372e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 7
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.342739e6

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 2.664e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.762e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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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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bin: 6.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.278e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 2.343514e6

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
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variant carriers: 10

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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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

Other
type: Population
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allele num: 908
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199652100890742e-4
allele num: 66686
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.999e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.99610253335332e-5
allele num: 66710
num of homozygotes: 0

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

South Asian
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Other
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.33e-1

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

GenotypeQuality
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variant carriers: 0

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

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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European (Non-Finnish)
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allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

European (Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
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allele num: 8650
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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QD
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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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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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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allele num: 11574
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VQSLOD
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FS
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MQRankSum
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DP
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 3.2e-2

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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European (Non-Finnish)
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allele num: 66692
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele num: 8650
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
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DP
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66694
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Other
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.856e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.983e1

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

European (Non-Finnish)
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South Asian
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African
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Latino
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Other
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East Asian
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allele frequency: 2.312138728323699e-4
allele num: 8650
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.342864e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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allele num: 6610
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Latino
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DP
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

Latino
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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South Asian
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 906
num of homozygotes: 0

Latino
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num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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African
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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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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East Asian
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Other
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African
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Latino
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allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.68e0

DP
type: SiteQuality
SIO_000300: 2.301275e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3817
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 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: 6602
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.010959894014212e-5
allele num: 66424
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1563e1

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: -1.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.59e-1

DP
type: SiteQuality
SIO_000300: 2.287277e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.309e1

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: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.064281382656155e-4
allele num: 6596
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.308e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.262558e6

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.231e1

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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variant carriers: 22

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1822
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variant carriers: 0

South Asian
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allele count: 11
allele frequency: 6.67637776159262e-4
allele num: 16476
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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: 11
allele frequency: 1.662334522154385e-4
allele num: 66172
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.254498e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
type: SiteQuality
SIO_000300: 6.037e1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

GenotypeQuality
all individuals: 737
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.331e0

VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

DP
type: SiteQuality
SIO_000300: 2.250877e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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MQRankSum
type: SiteQuality
SIO_000300: -1.855e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.648999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: -1.904e0

QD
type: SiteQuality
SIO_000300: 1.391e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.572e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.641276e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.693e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 906
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.642054e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.406e1

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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variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.647972e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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QD
type: SiteQuality
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InbreedingCoeff
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.002581109877247e-5
allele num: 66638
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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East Asian
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Other
type: Population
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VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

BaseQRankSum
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

FS
type: SiteQuality
SIO_000300: 4.543e0

DP
type: SiteQuality
SIO_000300: 2.65098e6

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66658
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
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DP
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SIO_000300: 2.654239e6

VQSLOD
type: SiteQuality
SIO_000300: 5.13e-1

ClippingRankSum
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SIO_000300: -8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 27732
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 10404
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.654642e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.382e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.052e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

QD
type: SiteQuality
SIO_000300: 1.427e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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bin: 2.5e0
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
all individuals: 2410
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.278e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.148e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.61e-1

FS
type: SiteQuality
SIO_000300: 2.98e0

DP
type: SiteQuality
SIO_000300: 2.65612e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.943e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.564e1

MQRankSum
type: SiteQuality
SIO_000300: -1.022e0

VQSLOD
type: SiteQuality
SIO_000300: -6.008e-1

DP
type: SiteQuality
SIO_000300: 2.656618e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.28e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

GenotypeQuality
all individuals: 4454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.99e0

QD
type: SiteQuality
SIO_000300: 1.533e1

VQSLOD
type: SiteQuality
SIO_000300: -1.235e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.646e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 2.656763e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5074
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.844675124951942e-4
allele num: 10404
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.224e1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.657385e6

FS
type: SiteQuality
SIO_000300: 1.336e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.171e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.55e-1

DP
type: SiteQuality
SIO_000300: 2.657276e6

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 8.58e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.337e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.657056e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.477e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.657448e6

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5082
bin: 6.75e1
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: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

FS
type: SiteQuality
SIO_000300: 8.91e-1

VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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SIO_000300: 5.95e1

MQRankSum
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SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

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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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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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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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.924e0

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

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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GenotypeQuality
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African
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allele num: 10406
num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

QD
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ClippingRankSum
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

DP
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 1.769e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 2.657504e6

QD
type: SiteQuality
SIO_000300: 1.16e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: -3.18e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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East Asian
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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

African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
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VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
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Other
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East Asian
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allele count: 10
allele frequency: 1.155802126675913e-3
allele num: 8652
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

African
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East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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Other
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

South Asian
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.656743e6

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

Latino
type: Population
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16510
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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QD
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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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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Other
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African
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South Asian
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.422e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 2.655244e6

VQSLOD
type: SiteQuality
SIO_000300: 1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.074e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

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

GenotypeQuality
all individuals: 27717
bin: 9.75e1
variant carriers: 16

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 111
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 13
allele frequency: 1.250240430852087e-3
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

QD
type: SiteQuality
SIO_000300: 1.614e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 1.879e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 2.654597e6

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2705
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5037
bin: 6.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.533e0

VQSLOD
type: SiteQuality
SIO_000300: -9.14e-2

QD
type: SiteQuality
SIO_000300: 1.546e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.653703e6

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
all individuals: 2413
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4399
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 4450
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variant carriers: 0

GenotypeQuality
all individuals: 2697
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variant carriers: 0

GenotypeQuality
all individuals: 9553
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.401392807828541e-4
allele num: 66628
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.382e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 2.651822e6

QD
type: SiteQuality
SIO_000300: 1.221e1

GenotypeQuality
all individuals: 9240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.987e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 1.675e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.264e0

QD
type: SiteQuality
SIO_000300: 1.235e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

DP
type: SiteQuality
SIO_000300: 2.644122e6

GenotypeQuality
all individuals: 2609
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
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variant carriers: 0

GenotypeQuality
all individuals: 4371
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variant carriers: 0

GenotypeQuality
all individuals: 4022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27664
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4759
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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: 904
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.425e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.343e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.406e-1

FS
type: SiteQuality
SIO_000300: 9.804e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e-1

DP
type: SiteQuality
SIO_000300: 2.631546e6

GenotypeQuality
all individuals: 4024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4357
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variant carriers: 0

GenotypeQuality
all individuals: 571
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 27662
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variant carriers: 1

GenotypeQuality
all individuals: 4758
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 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: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.552e1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

FS
type: SiteQuality
SIO_000300: 5.737e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 2.629468e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 308
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variant carriers: 0

GenotypeQuality
all individuals: 4011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 27685
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 1033
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 31
allele frequency: 1.879699248120301e-3
allele num: 16492
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.574807895133343e-4
allele num: 66370
num of homozygotes: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.211047420531526e-4
allele num: 11514
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.985e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

FS
type: SiteQuality
SIO_000300: 8.92e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

DP
type: SiteQuality
SIO_000300: 2.611728e6

GenotypeQuality
all individuals: 5836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 475
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4275
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GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 1169
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variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737921445950643e-4
allele num: 11508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.66e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

FS
type: SiteQuality
SIO_000300: 5.596e0

VQSLOD
type: SiteQuality
SIO_000300: -9.279999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

DP
type: SiteQuality
SIO_000300: 2.609786e6

GenotypeQuality
all individuals: 5497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 4274
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variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4271
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variant carriers: 0

GenotypeQuality
all individuals: 369
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variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4334
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variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 7.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66342
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.60925e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

GenotypeQuality
all individuals: 774
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
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variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5051
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8563
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21974
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

Latino
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allele frequency: 1.736111111111111e-4
allele num: 11520
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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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East Asian
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allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66088
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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DP
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VQSLOD
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MQ
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FS
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.739e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
allele num: 15854
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.681134613033378e-4
allele num: 65432
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.946375957572186e-4
allele num: 10182
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
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European (Finnish)
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allele count: 4
allele frequency: 6.257822277847309e-4
allele num: 6392
num of homozygotes: 0

ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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SIO_000300: 5.986e1

MQRankSum
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DP
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BaseQRankSum
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SIO_000300: -1.582e0

QD
type: SiteQuality
SIO_000300: 1.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.052e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 6.223549912870301e-5
allele num: 16068
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66152
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East Asian
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allele frequency: 0.0e0
allele num: 8582
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African
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.93e-1

ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.934e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
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SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16024
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.024711896191888e-5
allele num: 66122
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.755702e6

FS
type: SiteQuality
SIO_000300: 1.1354e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.228201295465869e-5
allele num: 16056
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66120
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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Other
type: Population
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ReadPosRankSum
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SIO_000300: 1.06e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
type: SiteQuality
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DP
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SIO_000300: 1.759751e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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African
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allele frequency: 6.76459219172787e-4
allele num: 10348
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Latino
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allele frequency: 8.662508662508663e-5
allele num: 11544
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6590
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66240
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
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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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European (Finnish)
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allele num: 6594
num of homozygotes: 0

Latino
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East Asian
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South Asian
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

DP
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ClippingRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

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

ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 900
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East Asian
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allele frequency: 3.472222222222222e-4
allele num: 8640
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Latino
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European (Non-Finnish)
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allele frequency: 4.521749615651282e-5
allele num: 66346
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European (Finnish)
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African
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South Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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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
all individuals: 30724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5010
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4365
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1327
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 2.051e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

DP
type: SiteQuality
SIO_000300: 1.783578e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

QD
type: SiteQuality
SIO_000300: 1.701e1

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

GenotypeQuality
all individuals: 31771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5011
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.327e1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.997e0

MQRankSum
type: SiteQuality
SIO_000300: 8.78e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.793678e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

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

GenotypeQuality
all individuals: 32369
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4391
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1842
bin: 9.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.105e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

FS
type: SiteQuality
SIO_000300: 2.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.102e1

DP
type: SiteQuality
SIO_000300: 1.802475e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-2