10-90770378-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770378
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770378
    reference: chr 10
allele count: 12
allele frequency: 9.901970492127933e-5
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.668+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.814+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.412+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.505+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.396+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.692A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.505+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.396+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.258+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.505+21A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000466081
  gene symbol: FAS
  hgvsc: ENST00000466081.1:n.586A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.654+21A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-90770390-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770390
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770390
    reference: chr 10
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.505+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.396+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.654+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.505+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.412+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.704C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.814+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.258+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000466081
  gene symbol: FAS
  hgvsc: ENST00000466081.1:n.598C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.668+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.396+33C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.505+33C>A
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

10-90770392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770392
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770392
    reference: chr 10
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.668+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.412+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000466081
  gene symbol: FAS
  hgvsc: ENST00000466081.1:n.600C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.505+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.505+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.505+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.706C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.396+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.814+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.654+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.396+35C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.258+35C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10557
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

10-90770401-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770401
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770401
    reference: chr 10
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.396+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.668+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000466081
  gene symbol: FAS
  hgvsc: ENST00000466081.1:n.609A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.258+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.396+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.715A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.505+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.505+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.412+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.814+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.505+44A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.654+44A>T
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD

10-90770466-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770466
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770466
    reference: chr 10
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+109G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.780G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+109G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+109G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-44G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-44G>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/10-90770467-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770467
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770467
    reference: chr 10
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+110A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+110A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.781A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+110A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-43A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-43A>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-90770483-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770483
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770483
    reference: chr 10
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+126T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+126T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+126T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.797T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-27T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-27T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-90770489-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770489
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770489
    reference: chr 10
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+132G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+132G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.803G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+132G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-21G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

10-90770496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770496
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770496
    reference: chr 10
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+139G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.810G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+139G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-14G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+139G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-90770499-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770499
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770499
    reference: chr 10
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+142C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+142C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.813C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-11C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+142C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-11C>G
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

10-90770499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770499
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770499
    reference: chr 10
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+142C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+142C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.813C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+142C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-11C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-11C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-90770505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770505
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770505
    reference: chr 10
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.259-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.506-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.413-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.397-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.506-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.819T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.815-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+148T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.655-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.397-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+148T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.506-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.669-5T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+148T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.506-5T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

10-90770528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770528
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770528
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.415G>A
  hgvsp: ENSP00000425159.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.673G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+171G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.415G>A
  hgvsp: ENSP00000423755.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.277G>A
  hgvsp: ENSP00000420975.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.431G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.687G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.524G>A
  hgvsp: ENSP00000345601.4:p.Gly175Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.833G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+171G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.524G>A
  hgvsp: ENSP00000347979.2:p.Gly175Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+171G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.524G>A
  hgvsp: ENSP00000347426.2:p.Gly175Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.842G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly175Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

10-90770529-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770529
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770529
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+172G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.674G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.416G>C
  hgvsp: ENSP00000425159.1:p.Gly139Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.688G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.843G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.432G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+172G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.525G>C
  hgvsp: ENST00000352159.4:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.278G>C
  hgvsp: ENSP00000420975.1:p.Gly93Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.525G>C
  hgvsp: ENST00000355279.2:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.416G>C
  hgvsp: ENSP00000423755.1:p.Gly139Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.525G>C
  hgvsp: ENST00000355740.2:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+172G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.834G>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly139Ala
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

10-90770537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770537
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770537
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.424G>A
  hgvsp: ENSP00000423755.1:p.Val142Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.533G>A
  hgvsp: ENSP00000347426.2:p.Cys178Tyr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.682G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+180G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.533G>A
  hgvsp: ENSP00000345601.4:p.Cys178Tyr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.286G>A
  hgvsp: ENSP00000420975.1:p.Val96Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.424G>A
  hgvsp: ENSP00000425159.1:p.Val142Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.851G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+180G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.842G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.440G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+180G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.533G>A
  hgvsp: ENSP00000347979.2:p.Cys178Tyr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.696G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys178Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-90770547-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770547
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770547
    reference: chr 10
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.861T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.434T>C
  hgvsp: ENSP00000425159.1:p.Phe145Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.543T>C
  hgvsp: ENST00000355279.2:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.450T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.852T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.543T>C
  hgvsp: ENST00000352159.4:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.543T>C
  hgvsp: ENST00000355740.2:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.434T>C
  hgvsp: ENSP00000423755.1:p.Phe145Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+190T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.296T>C
  hgvsp: ENSP00000420975.1:p.Phe99Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.706T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.692T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+190T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+190T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36113
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe145Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

10-90770552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770552
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770552
    reference: chr 10
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.548C>T
  hgvsp: ENSP00000347979.2:p.Pro183Leu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.548C>T
  hgvsp: ENSP00000345601.4:p.Pro183Leu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.857C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.439C>T
  hgvsp: ENSP00000425159.1:p.Gln147Ter
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.301C>T
  hgvsp: ENSP00000420975.1:p.Gln101Ter
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.455C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.697C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+195C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.439C>T
  hgvsp: ENSP00000423755.1:p.Gln147Ter
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.548C>T
  hgvsp: ENSP00000347426.2:p.Pro183Leu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.711C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+195C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.866C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+195C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36113
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln147Ter
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

10-90770553-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770553
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770553
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.712A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.867A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.549A>G
  hgvsp: ENST00000355740.2:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.858A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.549A>G
  hgvsp: ENST00000355279.2:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.698A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.549A>G
  hgvsp: ENST00000352159.4:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.440A>G
  hgvsp: ENSP00000425159.1:p.Gln147Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.440A>G
  hgvsp: ENSP00000423755.1:p.Gln147Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.302A>G
  hgvsp: ENSP00000420975.1:p.Gln101Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.456A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+196A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+196A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+196A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln147Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

10-90770554-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770554
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770554
    reference: chr 10
allele count: 116
allele frequency: 9.55487463345524e-4
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.713A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.303A>G
  hgvsp: ENST00000484444.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+197A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.550A>G
  hgvsp: ENSP00000347426.2:p.Ile184Val
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.859A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.550A>G
  hgvsp: ENSP00000345601.4:p.Ile184Val
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+197A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.457A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.441A>G
  hgvsp: ENST00000494410.1:c.441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.550A>G
  hgvsp: ENSP00000347979.2:p.Ile184Val
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.868A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.441A>G
  hgvsp: ENST00000488877.1:c.441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+197A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.699A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile184Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-90770564-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770564
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770564
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+207T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.709T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.467T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*1T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000477270
  gene symbol: FAS
  hgvsc: ENST00000477270.1:n.723T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+207T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+207T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*1T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.878T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.560T>C
  hgvsp: ENSP00000347426.2:p.Ile187Thr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.560T>C
  hgvsp: ENSP00000345601.4:p.Ile187Thr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*1T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.560T>C
  hgvsp: ENSP00000347979.2:p.Ile187Thr
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.869T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile187Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

10-90770579-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770579
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770579
    reference: chr 10
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+222T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.568+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*9+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.475+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.568+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.717+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+222T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.568+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*9+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+222T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.877+7T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.893T>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.568+7T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ

10-90770614-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770614
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770614
    reference: chr 10
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.568+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.717+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+257G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+257G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.568+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+257G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.928G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.877+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*9+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*9+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.568+42G>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.475+42G>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

10-90770620-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90770620
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90770620
    reference: chr 10
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.475+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000371857
  gene symbol: FAS
  hgvsc: ENST00000371857.3:n.934T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*9+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.258+263T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.568+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.505+263T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.396+263T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*9+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.568+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.877+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.717+48T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.568+48T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36110
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

10-90771718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771718
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771718
    reference: chr 10
allele count: 4
allele frequency: 3.342301843279467e-5
allele num: 119678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1146C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.569-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*10-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.878-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.506-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*10-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.569-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.476-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.569-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.397-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.259-38C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.718-38C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10889
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

10-90771726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771726
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771726
    reference: chr 10
allele count: 3
allele frequency: 2.503755633450175e-5
allele num: 119820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.259-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.506-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.718-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.476-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.878-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*10-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.569-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*10-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.569-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1154T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.569-30T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.397-30T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

10-90771731-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771731
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771730
    reference: chr 10
allele count: 1
allele frequency: 8.333055564814507e-6
allele num: 120004
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.569-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.397-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.506-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.569-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.878-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1160delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*10-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.476-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.259-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.718-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.569-24delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*10-24delG
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: TG
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

10-90771744-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771744
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771744
    reference: chr 10
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.569-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.506-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.718-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.878-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*10-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.569-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1172T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.476-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.397-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*10-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.259-12T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.569-12T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

10-90771746-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771746
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771746
    reference: chr 10
allele count: 2
allele frequency: 1.657687525901368e-5
allele num: 120650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.397-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.506-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*10-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.569-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.718-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.569-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.878-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.476-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*10-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.259-10G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1174G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.569-10G>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

10-90771762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771762
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771762
    reference: chr 10
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.884G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.482G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.575G>A
  hgvsp: ENSP00000347426.2:p.Arg192Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.575G>A
  hgvsp: ENSP00000347979.2:p.Arg192Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.575G>A
  hgvsp: ENSP00000345601.4:p.Arg192Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.512G>A
  hgvsp: ENSP00000349896.2:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.724G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1190G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg192Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

10-90771765-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771765
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771765
    reference: chr 10
allele count: 9
allele frequency: 7.434452906871087e-5
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.578A>G
  hgvsp: ENSP00000347979.2:p.Lys193Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.578A>G
  hgvsp: ENSP00000345601.4:p.Lys193Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.578A>G
  hgvsp: ENSP00000347426.2:p.Lys193Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.515A>G
  hgvsp: ENSP00000349896.2:p.Lys172Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.887A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1193A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.727A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.485A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys193Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

10-90771767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771767
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771767
    reference: chr 10
allele count: 218
allele frequency: 1.800730204358097e-3
allele num: 121062
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.889G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.517G>A
  hgvsp: ENSP00000349896.2:p.Glu173Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.729G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1195G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.580G>A
  hgvsp: ENSP00000347979.2:p.Glu194Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.580G>A
  hgvsp: ENSP00000345601.4:p.Glu194Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.487G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.580G>A
  hgvsp: ENSP00000347426.2:p.Glu194Lys
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10286
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu194Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

10-90771773-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771773
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771773
    reference: chr 10
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.895C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*15C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*27C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.735C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.523C>G
  hgvsp: ENSP00000349896.2:p.Gln175Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*27C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.586C>G
  hgvsp: ENSP00000345601.4:p.Gln196Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*15C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.586C>G
  hgvsp: ENSP00000347426.2:p.Gln196Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.586C>G
  hgvsp: ENSP00000347979.2:p.Gln196Glu
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1201C>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.493C>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln196Glu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-90771775-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771775
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771775
    reference: chr 10
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.588G>A
  hgvsp: ENST00000355740.2:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.495G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.737G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.588G>A
  hgvsp: ENST00000352159.4:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.588G>A
  hgvsp: ENST00000355279.2:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.897G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1203G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.525G>A
  hgvsp: ENST00000357339.2:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln196Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

10-90771782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771782
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771782
    reference: chr 10
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.595T>C
  hgvsp: ENSP00000347426.2:p.Cys199Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*24T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.532T>C
  hgvsp: ENSP00000349896.2:p.Cys178Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.595T>C
  hgvsp: ENSP00000347979.2:p.Cys199Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.904T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1210T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.595T>C
  hgvsp: ENSP00000345601.4:p.Cys199Arg
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.744T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*36T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*24T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*36T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.502T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys199Arg
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: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

10-90771795-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771795
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771795
    reference: chr 10
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*49G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.608G>T
  hgvsp: ENSP00000347426.2:p.Arg203Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.917G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.545G>T
  hgvsp: ENSP00000349896.2:p.Arg182Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.608G>T
  hgvsp: ENSP00000345601.4:p.Arg203Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.515G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.608G>T
  hgvsp: ENSP00000347979.2:p.Arg203Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1223G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*49G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.757G>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg203Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

10-90771800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771800
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771800
    reference: chr 10
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*54G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.762G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.922G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1228G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.613G>A
  hgvsp: ENSP00000347426.2:p.Glu205Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.520G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*54G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.613G>A
  hgvsp: ENSP00000347979.2:p.Glu205Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.613G>A
  hgvsp: ENSP00000345601.4:p.Glu205Lys
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.550G>A
  hgvsp: ENSP00000349896.2:p.Glu184Lys
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu205Lys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-90771817-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771817
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771817
    reference: chr 10
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*59T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.537T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.567T>C
  hgvsp: ENST00000357339.2:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*71T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*71T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.630T>C
  hgvsp: ENST00000352159.4:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.630T>C
  hgvsp: ENST00000355740.2:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1245T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*59T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.630T>C
  hgvsp: ENST00000355279.2:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.939T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.779T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His210His
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

10-90771824-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771824
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771824
    reference: chr 10
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.574C>T
  hgvsp: ENSP00000349896.2:p.Pro192Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*66C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1252C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.544C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*78C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.637C>T
  hgvsp: ENSP00000347979.2:p.Pro213Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.637C>T
  hgvsp: ENSP00000347426.2:p.Pro213Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.637C>T
  hgvsp: ENSP00000345601.4:p.Pro213Ser
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.946C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*78C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.786C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*66C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro213Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

10-90771827-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771827
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771827
    reference: chr 10
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.640A>G
  hgvsp: ENSP00000347979.2:p.Thr214Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*69A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.577A>G
  hgvsp: ENSP00000349896.2:p.Thr193Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.789A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.640A>G
  hgvsp: ENSP00000345601.4:p.Thr214Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.949A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*81A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.547A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.640A>G
  hgvsp: ENSP00000347426.2:p.Thr214Ala
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*81A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1255A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*69A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr214Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-90771828-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771828
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771828
    reference: chr 10
allele count: 7
allele frequency: 5.776912157924273e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*70C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1256C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.578C>A
  hgvsp: ENSP00000349896.2:p.Thr193Asn
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.641C>A
  hgvsp: ENSP00000345601.4:p.Thr214Asn
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.641C>A
  hgvsp: ENSP00000347979.2:p.Thr214Asn
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.641C>A
  hgvsp: ENSP00000347426.2:p.Thr214Asn
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*82C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.790C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.950C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*82C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.548C>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*70C>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr214Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

10-90771828-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771828
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771828
    reference: chr 10
allele count: 3
allele frequency: 2.47581949625326e-5
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1256C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.641C>T
  hgvsp: ENSP00000345601.4:p.Thr214Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.641C>T
  hgvsp: ENSP00000347979.2:p.Thr214Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.641C>T
  hgvsp: ENSP00000347426.2:p.Thr214Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.790C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.548C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.578C>T
  hgvsp: ENSP00000349896.2:p.Thr193Ile
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.950C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr214Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

10-90771829-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771829
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771829
    reference: chr 10
allele count: 91637
allele frequency: 7.561307677074395e-1
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*83T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.642T>C
  hgvsp: ENST00000352159.4:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*9+1257T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.549T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.951T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.791T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.642T>C
  hgvsp: ENST00000355279.2:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*83T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.642T>C
  hgvsp: ENST00000355740.2:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*71T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.579T>C
  hgvsp: ENST00000357339.2:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*71T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 3.75e1
  variant carriers: 1507
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.75e1
  variant carriers: 594
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 6.75e1
  variant carriers: 4344
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 4.75e1
  variant carriers: 3067
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.25e1
  variant carriers: 2204
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 4.25e1
  variant carriers: 2279
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.25e1
  variant carriers: 4475
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.75e1
  variant carriers: 3706
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 8.75e1
  variant carriers: 2681
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 8.25e1
  variant carriers: 3208
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 5.25e1
  variant carriers: 3839
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 5.75e1
  variant carriers: 4255
genotype quality: GenotypeQuality
hgvs: p.Thr214Thr
num of homozygotes: 35133
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

10-90771841-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771841
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771840
    reference: chr 10
allele count: 1
allele frequency: 8.295037908323241e-6
allele num: 120554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+5delG
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1257delG
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.651+5delG
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: AG
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

10-90771845-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771845
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771845
    reference: chr 10
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1255A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+7A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+7A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.651+7A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-90771846-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771846
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771846
    reference: chr 10
allele count: 4
allele frequency: 3.322314324158209e-5
allele num: 120398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1254T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+8T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+8T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.651+8T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

10-90771854-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771854
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771854
    reference: chr 10
allele count: 1
allele frequency: 8.332500083325001e-6
allele num: 120012
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1246G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+16G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+16G>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-90771855-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771855
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771855
    reference: chr 10
allele count: 1
allele frequency: 8.339448929214757e-6
allele num: 119912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1245G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+17G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+17G>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

10-90771875-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771875
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771875
    reference: chr 10
allele count: 1
allele frequency: 8.508031581813232e-6
allele num: 117536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1225G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+37G>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+37G>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

10-90771881-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90771881
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90771881
    reference: chr 10
allele count: 743
allele frequency: 6.338184361830993e-3
allele num: 117226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000487314
  gene symbol: FAS
  hgvsc: ENST00000487314.1:n.800+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.588+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.960+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.651+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-1219T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*80+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.651+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.558+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*80+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*92+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*92+43T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.651+43T>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 17967
  bin: 2.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 3.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 28
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

10-90773049-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773049
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773049
    reference: chr 10
allele count: 1
allele frequency: 8.388276544701125e-6
allele num: 119214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-827T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-51T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-51T>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-90773058-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773058
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773059
    reference: chr 10
allele count: 2
allele frequency: 1.67596829067994e-5
allele num: 119334
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-813dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-37dupT
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-37dupT
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP

10-90773059-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773059
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773059
    reference: chr 10
allele count: 5
allele frequency: 4.187955440154116e-5
allele num: 119390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-817T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-41T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-41T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

10-90773064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773064
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773064
    reference: chr 10
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-812A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-36A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

10-90773065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773065
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773065
    reference: chr 10
allele count: 2
allele frequency: 1.670090351888037e-5
allele num: 119754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-811T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-35T>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-35T>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD

10-90773082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773082
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773082
    reference: chr 10
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-794C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-18C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-18C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-90773092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773092
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773092
    reference: chr 10
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*93-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.961-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.652-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.559-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.652-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.589-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*10-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*93-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-784C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*81-8C>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*81-8C>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.652-8C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-90773106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773106
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773106
    reference: chr 10
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.658G>A
  hgvsp: ENSP00000347979.2:p.Val220Met
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*87G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.565G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.595G>A
  hgvsp: ENSP00000349896.2:p.Val199Met
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*87G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.658G>A
  hgvsp: ENSP00000345601.4:p.Val220Met
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-770G>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.967G>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val220Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

10-90773114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773114
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773114
    reference: chr 10
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.573A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.603A>G
  hgvsp: ENSP00000349896.2:p.Ile201Met
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.975A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*95A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*95A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*24A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.666A>G
  hgvsp: ENSP00000347979.2:p.Ile222Met
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-762A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.666A>G
  hgvsp: ENSP00000345601.4:p.Ile222Met
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile222Met
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/10-90773115-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773115
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773115
    reference: chr 10
allele count: 10
allele frequency: 8.284180528862085e-5
allele num: 120712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*96A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.667A>C
  hgvsp: ENSP00000347979.2:p.Asn223His
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.667A>C
  hgvsp: ENSP00000345601.4:p.Asn223His
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*108A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.574A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*25A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*96A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.976A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.604A>C
  hgvsp: ENSP00000349896.2:p.Asn202His
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*108A>C
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-761A>C
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn223His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-90773132-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773132
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773132
    reference: chr 10
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-744T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+8T>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+8T>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.676+8T>G
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

10-90773136-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773136
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773136
    reference: chr 10
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-740A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+12A>T
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+12A>T
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9410
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

10-90773146-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773146
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773146
    reference: chr 10
allele count: 77
allele frequency: 6.377656666721885e-4
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+22T>A
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-730T>A
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-90773149-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773149
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773149
    reference: chr 10
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-727A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+25A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+25A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

10-90773151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773151
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773151
    reference: chr 10
allele count: 2
allele frequency: 1.656781205474005e-5
allele num: 120716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-725A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+27A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+27A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

10-90773153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773153
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773153
    reference: chr 10
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-723A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+29A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+29A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

10-90773160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773160
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773160
    reference: chr 10
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  hgvsc: ENST00000355740.2:c.676+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  hgvsc: ENST00000492756.1:c.*105+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  hgvsc: ENST00000352159.4:c.676+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  hgvsc: ENST00000494410.1:c.*34+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  hgvsc: ENST00000313771.5:n.985+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  hgvsc: ENST00000494799.1:n.583+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  hgvsc: ENST00000488877.1:c.*117+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  hgvsc: ENST00000479522.1:c.*105+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  hgvsc: ENST00000357339.2:c.613+36A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  hgvsc: ENST00000355279.2:c.652-716A>G
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  hgvsc: ENST00000484444.1:c.*117+36A>G
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

10-90773164-T-TTCCAACCTACAGGATCCAGATCTAAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 90773164
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 90773190
    reference: chr 10
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: TTCCAACCTACAGGATCCAGATCTAAC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000423755
  ensembl transcript: ENST00000494410
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000425159
  ensembl transcript: ENST00000488877
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000422453
  ensembl transcript: ENST00000492756
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000345601
  ensembl transcript: ENST00000352159
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000349896
  ensembl transcript: ENST00000357339
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347979
  ensembl transcript: ENST00000355740
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000347426
  ensembl transcript: ENST00000355279
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000494799
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000420975
  ensembl transcript: ENST00000484444
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl protein: ENSP00000424113
  ensembl transcript: ENST00000479522
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000026103
  ensembl transcript: ENST00000313771
  gene symbol: FAS
  variant of: http://identifiers.org/hgnc/11920
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 7615
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1657
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1336
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10541
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2185
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 623
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2889
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4039
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1805
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16516
bin: 9.75e1
variant carriers: 12

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

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.799694052011158e-4
allele num: 66678
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

DP
type: SiteQuality
SIO_000300: 2.455154e6

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.409e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 20716
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 228
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1037
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2889
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1660
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21777
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16529
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1824
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6720
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3460
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
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: 11452
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

FS
type: SiteQuality
SIO_000300: 1.834e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.718e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.38e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 2.45741e6

GenotypeDepth
all individuals: 4095
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20675
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 815
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7655
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1037
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2889
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16543
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 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: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.528e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.059e0

FS
type: SiteQuality
SIO_000300: 6.282e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 2.458216e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4116
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2202
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1664
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1344
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16576
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

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

QD
type: SiteQuality
SIO_000300: 3.435e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.51e-2

DP
type: SiteQuality
SIO_000300: 2.459738e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: -1.537e-1

GenotypeDepth
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1056
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3769
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2114
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.609840476648087e-5
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: 11532
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66732
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
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
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
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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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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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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 num: 16510
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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SIO_000300: 1.86e-1

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

European (Finnish)
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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

European (Non-Finnish)
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allele count: 1
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allele num: 66738
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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num of homozygotes: 0

East Asian
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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 count: 1
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allele num: 66740
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African
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European (Finnish)
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South Asian
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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QD
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DP
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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Other
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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MQRankSum
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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allele count: 1
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.465e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 2.23e0

QD
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SIO_000300: 1.455e1

BaseQRankSum
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DP
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SIO_000300: 6.455699e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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South Asian
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MQ
type: SiteQuality
SIO_000300: 5.964e1

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

ReadPosRankSum
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SIO_000300: 5.679999999999999e-1

MQ
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SIO_000300: 5.942e1

QD
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ClippingRankSum
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SIO_000300: -5.8e-2

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 6.45571e6

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.274e0

BaseQRankSum
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SIO_000300: -1.064e0

MQRankSum
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SIO_000300: 7.72e-1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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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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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
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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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num of homozygotes: 0

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

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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Other
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Latino
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QD
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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European (Finnish)
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Latino
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Other
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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QD
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FS
type: SiteQuality
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 2.996703626011388e-5
allele num: 66740
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Latino
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African
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Other
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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East Asian
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QD
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FS
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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South Asian
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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Latino
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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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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African
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East Asian
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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DP
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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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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bin: 3.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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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 frequency: 6.069065970747102e-5
allele num: 65908
num of homozygotes: 0

Other
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 6.919999999999999e-1

MQ
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SIO_000300: 5.919e1

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

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

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

Other
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num of homozygotes: 0

Latino
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allele frequency: 2.638058389025677e-4
allele num: 11372
num of homozygotes: 0

African
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South 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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MQRankSum
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SIO_000300: 1.02e-1

BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66110
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African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 2.62e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506114826194349e-5
allele num: 66396
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 0.0e0

QD
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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SIO_000300: 9.370000000000001e-1

VQSLOD
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SIO_000300: 1.48e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11430
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.010144185906505e-5
allele num: 66442
num of homozygotes: 0

Other
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African
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VQSLOD
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DP
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16500
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European (Finnish)
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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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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

African
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66608
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Other
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Latino
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allele num: 11458
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European (Finnish)
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 5423
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 175
allele frequency: 2.62731203459044e-3
allele num: 66608
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.724480893386843e-4
allele num: 11462
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.575757575757576e-3
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.894635275955229e-4
allele num: 10364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

InbreedingCoeff
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SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

DP
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SIO_000300: 2.416504e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

FS
type: SiteQuality
SIO_000300: 2.722e0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11462
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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.34e-1

FS
type: SiteQuality
SIO_000300: 2.06e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
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SIO_000300: 2.413309e6

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 5.962e1

ClippingRankSum
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SIO_000300: 1.38e0

QD
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SIO_000300: 1.353e1

BaseQRankSum
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SIO_000300: -6.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-1

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

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

African
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allele count: 1
allele frequency: 9.641342074816814e-5
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.347e0

ClippingRankSum
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SIO_000300: 1.02e0

QD
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SIO_000300: 1.175e1

BaseQRankSum
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SIO_000300: -1.96e0

FS
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SIO_000300: 6.898e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 2.413527e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 156
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GenotypeQuality
all individuals: 35
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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: 8632
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 1.852e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

DP
type: SiteQuality
SIO_000300: 2.413999e6

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.505e1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3063
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GenotypeQuality
all individuals: 145
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
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: 8638
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 3.283e0

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

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

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

Latino
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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: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.192e0

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

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

Other
type: Population
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66662
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African
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European (Finnish)
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South Asian
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East Asian
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

Latino
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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: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 1.788e0

ReadPosRankSum
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SIO_000300: -1.7e-2

DP
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SIO_000300: 2.415793e6

MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.509e-1

GenotypeDepth
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variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 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: 11484
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

QD
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SIO_000300: 1.09e1

VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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SIO_000300: 5.69e-1

ClippingRankSum
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SIO_000300: 1.17e0

MQ
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SIO_000300: 5.949e1

FS
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SIO_000300: 2.709e0

DP
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SIO_000300: 2.416103e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5444
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.105604446503011e-4
allele num: 8636
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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -3.269e0

MQ
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SIO_000300: 5.976e1

ReadPosRankSum
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SIO_000300: 6.900000000000001e-2

DP
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SIO_000300: 2.416861e6

ClippingRankSum
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SIO_000300: -1.49e-1

InbreedingCoeff
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SIO_000300: 2.7e-3

FS
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.221e1

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 154
bin: 5.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817741153659719e-4
allele num: 16504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

ReadPosRankSum
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SIO_000300: 6.900000000000001e-2

QD
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SIO_000300: 1.221e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
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SIO_000300: 2.7e-3

MQRankSum
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SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

DP
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SIO_000300: 2.416861e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.269e0

GenotypeDepth
all individuals: 1575
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variant carriers: 945

GenotypeDepth
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variant carriers: 4063

GenotypeDepth
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variant carriers: 14645

GenotypeQuality
all individuals: 92
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variant carriers: 83

GenotypeQuality
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GenotypeQuality
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variant carriers: 108

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 55262

GenotypeQuality
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variant carriers: 240

GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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GenotypeQuality
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variant carriers: 43

GenotypeQuality
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variant carriers: 50

GenotypeQuality
all individuals: 171
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variant carriers: 126

GenotypeQuality
all individuals: 240
bin: 7.25e1
variant carriers: 73

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 57

European (Non-Finnish)
type: Population
allele count: 46565
allele frequency: 6.987545018007203e-1
allele num: 66640
num of homozygotes: 16231

European (Finnish)
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allele count: 5242
allele frequency: 7.930408472012103e-1
allele num: 6610
num of homozygotes: 2087

East Asian
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allele count: 8508
allele frequency: 9.831291888144211e-1
allele num: 8654
num of homozygotes: 4183

African
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allele count: 7014
allele frequency: 6.762437331276514e-1
allele num: 10372
num of homozygotes: 2363

South Asian
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allele count: 13633
allele frequency: 8.261422857835414e-1
allele num: 16502
num of homozygotes: 5662

Latino
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allele count: 9972
allele frequency: 8.665276329509907e-1
allele num: 11508
num of homozygotes: 4335

Other
type: Population
allele count: 703
allele frequency: 7.759381898454746e-1
allele num: 906
num of homozygotes: 272

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
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DP
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BaseQRankSum
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MQ
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SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.53e-2

FS
type: SiteQuality
SIO_000300: 6.02e-1

QD
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SIO_000300: 2.799e1

ReadPosRankSum
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SIO_000300: 3.26e-1

GenotypeDepth
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variant carriers: 0

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

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

Latino
type: Population
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: 1.507068149621726e-5
allele num: 66354
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

DP
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FS
type: SiteQuality
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MQRankSum
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MQ
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SIO_000300: 5.922e1

BaseQRankSum
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SIO_000300: 9.0e-2

InbreedingCoeff
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SIO_000300: 1.1e-3

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.773469029654326e-5
allele num: 11398
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 863
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GenotypeQuality
all individuals: 1935
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.781173164734808e-5
allele num: 11388
num of homozygotes: 0

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

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

African
type: Population
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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
allele num: 8510
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: 3
allele frequency: 4.526252263126132e-5
allele num: 66280
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 2.13e-1

QD
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FS
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ClippingRankSum
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DP
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SIO_000300: 2.098049e6

BaseQRankSum
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SIO_000300: 4.66e0

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 31
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66062
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
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SIO_000300: 4.53e-1

ReadPosRankSum
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SIO_000300: 9.379999999999999e-1

BaseQRankSum
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SIO_000300: -2.458e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

DP
type: SiteQuality
SIO_000300: 2.087722e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514738404677512e-5
allele num: 66018
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.921e1

ReadPosRankSum
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SIO_000300: 1.78e0

BaseQRankSum
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SIO_000300: -1.34e0

FS
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SIO_000300: 4.355e0

MQRankSum
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SIO_000300: 2.76e-1

VQSLOD
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SIO_000300: 1.58e-1

ClippingRankSum
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SIO_000300: -4.97e-1

DP
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SIO_000300: 2.084825e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.454e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10020
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.984025559105431e-5
allele num: 10016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.947697e6

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.81e-1

BaseQRankSum
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SIO_000300: -2.157e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeDepth
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variant carriers: 29

GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 710

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1731
bin: 8.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 101
allele frequency: 1.567495421671788e-3
allele num: 64434
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.643340857787811e-3
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.805054151624549e-4
allele num: 11080
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.006018054162487e-4
allele num: 9970
num of homozygotes: 0

South Asian
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allele count: 15
allele frequency: 9.200196270853779e-4
allele num: 16304
num of homozygotes: 0

East Asian
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allele count: 557
allele frequency: 6.955544455544456e-2
allele num: 8008
num of homozygotes: 27

European (Finnish)
type: Population
allele count: 61
allele frequency: 9.321515892420537e-3
allele num: 6544
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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DP
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VQSLOD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 4.4e0

MQRankSum
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SIO_000300: 1.73e-1

ClippingRankSum
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SIO_000300: 6.1e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084205402774397e-5
allele num: 16436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.631e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
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SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 2.471591e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.0e0

MQ
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SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.139e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.64e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28618
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.215509906405737e-4
allele num: 16454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65496
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10002
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
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VQSLOD
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SIO_000300: 1.6e0

MQ
type: SiteQuality
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MQRankSum
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SIO_000300: 1.97e0

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.195e1

BaseQRankSum
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SIO_000300: 9.2e-2

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

Latino
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allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 7.62939453125e-5
allele num: 65536
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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VQSLOD
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QD
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FS
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

DP
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SIO_000300: 2.501556e6

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521792062332603e-5
allele num: 65712
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
type: Population
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Latino
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 3.7e-3

DP
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SIO_000300: 2.51376e6

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

European (Non-Finnish)
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allele num: 65812
num of homozygotes: 0

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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Latino
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South Asian
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Other
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BaseQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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FS
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MQ
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VQSLOD
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SIO_000300: -2.032e0

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

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

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

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

African
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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
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50934283213089e-5
allele num: 66254
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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DP
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QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

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

Latino
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allele num: 11428
num of homozygotes: 0

Other
type: Population
allele count: 0
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African
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DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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ClippingRankSum
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SIO_000300: -5.86e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

African
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East Asian
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allele num: 8622
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European (Finnish)
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 10

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.811616954474098e-5
allele num: 10192
num of homozygotes: 0

South Asian
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allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.033423667570009e-5
allele num: 66420
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.32e0

InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: 1.99e0

QD
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MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
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SIO_000300: 2.532886e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.61e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

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

East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66444
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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SIO_000300: -5.1e-2

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

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

Latino
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allele frequency: 8.724480893386844e-5
allele num: 11462
num of homozygotes: 0

South Asian
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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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Other
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African
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ReadPosRankSum
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SIO_000300: -1.808e0

BaseQRankSum
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DP
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MQRankSum
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SIO_000300: -6.33e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.08e0

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.834e-1

ClippingRankSum
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SIO_000300: 1.75e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 77

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

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

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

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

Latino
type: Population
allele count: 77
allele frequency: 6.720195496596265e-3
allele num: 11458
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Other
type: Population
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
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MQ
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SIO_000300: 5.974e1

VQSLOD
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FS
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BaseQRankSum
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SIO_000300: -2.255e0

InbreedingCoeff
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SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.235e1

DP
type: SiteQuality
SIO_000300: 2.532885e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 3111
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.825112988799372e-5
allele num: 10178
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

South Asian
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East Asian
type: Population
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num of homozygotes: 0

Other
type: Population
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FS
type: SiteQuality
SIO_000300: 1.444e0

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.961e1

VQSLOD
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ClippingRankSum
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DP
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QD
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SIO_000300: 1.331e1

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

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.964636542239686e-4
allele num: 10180
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

MQRankSum
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QD
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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SIO_000300: 5.53e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16500
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Other
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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South Asian
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African
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allele frequency: 9.827044025157233e-5
allele num: 10176
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Latino
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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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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

FS
type: SiteQuality
SIO_000300: 3.581e0

DP
type: SiteQuality
SIO_000300: 2.527738e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.024e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1